EP2082205B1 - Transducteur destiné à être utilisé dans des environnements hostiles - Google Patents

Transducteur destiné à être utilisé dans des environnements hostiles Download PDF

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Publication number
EP2082205B1
EP2082205B1 EP07814915.0A EP07814915A EP2082205B1 EP 2082205 B1 EP2082205 B1 EP 2082205B1 EP 07814915 A EP07814915 A EP 07814915A EP 2082205 B1 EP2082205 B1 EP 2082205B1
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EP
European Patent Office
Prior art keywords
layer
substrate
sensor
materials
diaphragm
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Application number
EP07814915.0A
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German (de)
English (en)
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EP2082205A2 (fr
Inventor
Odd Harald Steen Eriksen
Kimiko J. Childress
Shuwen Guo
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Rosemount Aerospace Inc
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Rosemount Aerospace Inc
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Publication of EP2082205A2 publication Critical patent/EP2082205A2/fr
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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01L—MEASURING FORCE, STRESS, TORQUE, WORK, MECHANICAL POWER, MECHANICAL EFFICIENCY, OR FLUID PRESSURE
    • G01L9/00—Measuring steady of quasi-steady pressure of fluid or fluent solid material by electric or magnetic pressure-sensitive elements; Transmitting or indicating the displacement of mechanical pressure-sensitive elements, used to measure the steady or quasi-steady pressure of a fluid or fluent solid material, by electric or magnetic means
    • G01L9/0041—Transmitting or indicating the displacement of flexible diaphragms
    • G01L9/0042—Constructional details associated with semiconductive diaphragm sensors, e.g. etching, or constructional details of non-semiconductive diaphragms
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/02—Pretreatment of the material to be coated
    • C23C14/021—Cleaning or etching treatments
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/02—Pretreatment of the material to be coated
    • C23C14/021—Cleaning or etching treatments
    • C23C14/022—Cleaning or etching treatments by means of bombardment with energetic particles or radiation
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
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    • C23C14/024—Deposition of sublayers, e.g. to promote adhesion of the coating
    • C23C14/025—Metallic sublayers
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/0682—Silicides
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    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
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    • C23C14/5806—Thermal treatment
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
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    • C23C14/5846—Reactive treatment
    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00—Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
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    • G—PHYSICS
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    • G01L19/0061—Electrical connection means
    • G—PHYSICS
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    • G01L19/0069—Electrical connection means from the sensor to its support
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    • G01L19/0069—Electrical connection means from the sensor to its support
    • G01L19/0076—Electrical connection means from the sensor to its support using buried connections
    • G—PHYSICS
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    • G01L19/00—Details of, or accessories for, apparatus for measuring steady or quasi-steady pressure of a fluent medium insofar as such details or accessories are not special to particular types of pressure gauges
    • G01L19/06—Means for preventing overload or deleterious influence of the measured medium on the measuring device or vice versa
    • G01L19/0609—Pressure pulsation damping arrangements
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    • G01L19/141—Monolithic housings, e.g. molded or one-piece housings
    • G—PHYSICS
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    • G—PHYSICS
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    • G01L9/00—Measuring steady of quasi-steady pressure of fluid or fluent solid material by electric or magnetic pressure-sensitive elements; Transmitting or indicating the displacement of mechanical pressure-sensitive elements, used to measure the steady or quasi-steady pressure of a fluid or fluent solid material, by electric or magnetic means
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    • G01L9/0054—Transmitting or indicating the displacement of flexible diaphragms using variations in ohmic resistance of piezoresistive elements integral with a semiconducting diaphragm
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    • G01L9/0041—Transmitting or indicating the displacement of flexible diaphragms
    • G01L9/008—Transmitting or indicating the displacement of flexible diaphragms using piezoelectric devices
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    • H01L2224/04—Structure, shape, material or disposition of the bonding areas prior to the connecting process
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    • H01L2224/01—Means for bonding being attached to, or being formed on, the surface to be connected, e.g. chip-to-package, die-attach, "first-level" interconnects; Manufacturing methods related thereto
    • H01L2224/42—Wire connectors; Manufacturing methods related thereto
    • H01L2224/44—Structure, shape, material or disposition of the wire connectors prior to the connecting process
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    • H01L2224/451—Material with a principal constituent of the material being a metal or a metalloid, e.g. boron (B), silicon (Si), germanium (Ge), arsenic (As), antimony (Sb), tellurium (Te) and polonium (Po), and alloys thereof
    • H01L2224/45163—Material with a principal constituent of the material being a metal or a metalloid, e.g. boron (B), silicon (Si), germanium (Ge), arsenic (As), antimony (Sb), tellurium (Te) and polonium (Po), and alloys thereof the principal constituent melting at a temperature of greater than 1550°C
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Definitions

  • the present invention is directed to transducer for use in harsh environments, and more particularly, to a transducer, such as a sensor or actuator, which is configured to withstand high temperatures and corrosive environments.
  • Transducers such as sensor or actuators
  • a microphone or dynamic pressure sensor in or adjacent to the combustion zone of a turbine, aircraft engine or internal combustion engine to detect dynamic pressure changes inside the turbine or engine.
  • the dynamic pressure data can then be analyzed to track the efficiency and performance of the turbine or engine.
  • the dynamic pressure sensor may also be utilized to track the acoustic characteristics of the turbine or engine (i.e., noise output).
  • the transducer must be able to withstand high operating temperatures and pressures, wide ranges of temperature and pressure, and the presence of combustion byproducts.
  • the transducer is a MEMS (microelectromechanical system) device
  • the MEMS transducer may be susceptible to damage due to its inherent materials of manufacture, thereby requiring additional protection.
  • US6122974 describes a pressure sensor having plural pressure sensing sections for for high and low pressures, each section comprising an outer frame portion, a diaphragm portion, a strain gauge portion, and an electrode portion.
  • EP0585084 describes techniques for forming permanent joints between two bodies or devices using metallic bonding materials and
  • US2005/0224966 describes interconnecting microelectronic integrated circuit chips to packages using lead-free solder alloys and environmentally benign fabrication technologies.
  • US 2005/0235753 discloses a sensor which comprises a leadless high sensitivity differential transducer chip which responds to both static and dynamic pressure.
  • the transducer is typically electrically connected to an external device, controller or the like.
  • the associated connections must also therefore be protected from the harsh environment to ensure proper operation of the transducer. Accordingly, there is a need for an improved transducer which can withstand such harsh environments.
  • the invention provides a pressure sensor for use in harsh environments as set out in the accompanying claims.
  • the present invention is a pressure sensor which can withstand harsh environments.
  • the pressure sensor includes electrical connections that are fluidly isolated to protect the electrical connection from the surrounding harsh environment.
  • the invention is a pressure sensor for use in a harsh environment including a substrate and a sensor die directly coupled to the substrate by a bond frame positioned between the substrate and the sensor die.
  • the sensor die includes a sensing element which provides an output signal related to a physical characteristic to be measured, or which receives an input signal and responsively provides a physical output.
  • the sensor further includes a connecting component electrically coupled to an output contact (which is electrically coupled to the sensing element) at a connection location that is fluidly isolated from the sensing element by the bond frame.
  • the bond frame is made of materials and the connecting component is electrically coupled to the sensing element by the same materials of the bond frame.
  • one embodiment of the transducer takes the form of a pressure sensor 10, such as a dynamic pressure sensor or microphone which can be used to sense rapid pressure fluctuations in the surrounding fluid.
  • the pressure sensor 10 may be configured to be mounted in or adjacent to the combustion cavity of an engine, such as a turbine, aircraft engine or internal combustion engine. In this case, the pressure sensor 10 may be configured to withstand relatively high operating temperatures, wide temperature ranges, high operating pressure, and the presence of combustion byproducts (such as water, CO, CO 2 , NO x , and various nitrous and sulfurous compounds).
  • the illustrated sensor 10 includes a transducer die or sensor die 12 electrically and mechanically coupled to an underlying substrate 14.
  • the sensor die 12 includes a diaphragm/ membrane 16 and is configured to measure dynamic differential pressure across the diaphragm 16.
  • the materials of the sensor die 12 and substrate 14 will be discussed in detail below, but in one embodiment the sensor die 12 includes or is made of a semiconductor-on-insulator wafer or a silicon-on-insulator ("SOI") wafer.
  • the substrate 14 may be a generally disk-shaped ceramic material that is compression mounted inside a thin walled metal ring 18.
  • the ring 18 is, in turn, mounted to a header, header plate, base or pedestal 20 which provides support to the ring 18 and structure and protection to the sensor 10 as a whole.
  • the diaphragm 16 can be made of a variety of materials, such as semiconductor materials, but in one case is made of nearly any non-metallic material.
  • the wire 24 can then be connected to an external controller, processor, amplifier, charge converter or the like to thereby communicate the output of the sensor die 12.
  • a screen 26 may be provided across the upper opening of the base 20 to provide some mechanical protection to the sensor die 12, and also to provide protection from fluidic and thermal spikes.
  • the sensor die 12 may be made of or include a SOI wafer 30.
  • the wafer 30 includes a base or handle layer of silicon 32, an upper or device layer of silicon 34, and an oxide or electrically insulating layer 36 positioned between the device layer 34 and base layer 32.
  • the device layer 34 may be an electrically conductive material such as doped silicon.
  • the SOI wafer 30/device layer 34 may be made of various other materials besides silicon. Portions of the base layer 32 and the oxide layer 36 are removed to expose portions of the device layer 34 to thereby form the diaphragm 16 which can flex in response to differential pressure thereacross.
  • the sensor 10 includes a piezoelectric sensing element, generally designated 40, which includes a piezoelectric film 42 located over the device layer 34/diaphragm 16.
  • a set of electrodes 44, 46 are positioned on the piezoelectric film 42.
  • a dielectric or passivation layer 48 may be located over the electrodes 44, 46 and piezoelectric film 42 to protect those components.
  • Fig. 3 illustrates one configuration for the electrodes wherein the sensor die 12 includes a center electrode 44 and an outer electrode 46 located generally about the center electrode 44, with a gap 49 positioned between the electrodes 44, 46.
  • the center electrode 44 is configured to be located over areas of tensile surface strain of the diaphragm 16 when the diaphragm 16 is deflected (i.e., due to differential pressure), and the outer electrode 46 is positioned to be located over areas of compressive surface strain of the diaphragm 46 when the diaphragm 46 is deflected.
  • the gap 49 between the center 44 and outer 46 electrodes is located on a region of minimal or no strain when the diaphragm 16 is flexed.
  • the sensor die 12 of Fig. 3 includes a pair of output contacts 50, 52, with each output contact 50, 52 being directly electrically coupled to one of the electrodes 44, 46.
  • lead 56 extends from the center electrode 44 to the output contact 50 to electrically connect those components
  • lead 58 extends from the outer electrode 46 to the output contact 52 to electrically connect those components.
  • Both leads 56, 58 may be "buried" leads that are located between the dielectric layer 48 and the piezoelectric film 42 (i.e., see lead 58 of Fig. 4 ).
  • an insulating layer (not shown) may be deposited on the sensor 12 and positioned between the leads 56, 58 and the device layer 34 to electrically isolate the leads 56, 58 from the device layer 34.
  • the sensor die 12 may also include a reference contact 60 which extends through the piezoelectric film 42 to directly contact the device layer 34 (see Fig. 4 ).
  • the reference contact 60 provides a reference or "ground” voltage which can be compared to voltages measured at the contacts 50, 52.
  • the reference contact 60 may be omitted in which case the induced piezoelectric charge relative to the electrodes 44, 46 is measured using a charge converter or charge amplifier.
  • the diaphragm 16 In operation, when the sensor die 12 is exposed to differing pressures across the diaphragm 16, the diaphragm 16 is bowed either upwardly or downwardly from the position shown in Fig. 4 .
  • downward deflection of the diaphragm 16 occurs when a relatively higher pressure is located on the top side of the diaphragm 16, thereby causing tensile strain to be induced in portions of the piezoelectric film 42 located adjacent to the center electrode 44.
  • a compressive strain is induced in the portions of the piezoelectric film 42 located adjacent to the outer electrode 46.
  • the induced stresses cause change in the electric characteristics (i.e.
  • the substrate 14 may include a depression 62 formed on an upper surface thereof to accommodate downward deflection of the diaphragm 16.
  • the depression 62 is optional and may be omitted if desired.
  • the electrodes 44, 46 and leads 56, 58 accumulate and transmit the induced piezoelectric charge to the contacts 50, 52. From there the contacts 50, 52 allow the charge to be transmitted (via pins 22 and wires 24) to a charge converter or charge amplifier, and ultimately a controller, processor or the like which can process the output to determine the sensed pressure/pressure change.
  • the piezoelectric film 42 provides a very fast response time and therefore is useful in measuring vibration and other high frequency phenomenon.
  • the piezoelectric film 42 is typically used in sensing dynamic or A/C or high-frequency pressure changes.
  • the utility of piezoelectric film to sense static or D/C or low-frequency pressure changes is typically limited due to leakback effects related to dielectric leakage through the piezoelectric film.
  • the sensing element 40 may use a piezoresistive film.
  • the piezoresistive film can accurately sense static or D/C or low-frequency pressure changes.
  • the piezoresistive film is patterned in a serpentine shape as shown in Fig. 43 in the well known manner on the diaphragm 16 and electrically coupled to the contacts 50, 52 in a well known manner.
  • the serpentine pattern may form a Wheatstone bridge configuration whereby two legs of the Wheatstone bridge are located over the diaphragm 16. The deflection of the diaphragm 16 is then measured through a change in resistance of the piezoresistive film in a well known manner.
  • the piezoelectric sensing element 40 may have a variety of shapes and configurations different from that specifically shown herein.
  • the diaphragm 16, center electrode 44 and outer electrode 46 may each have a circular shape or other shapes in top view, rather than a square or rectangular shape.
  • a single sensing electrode 44 may be utilized.
  • the single electrode 44 may be located over only the inner (or outer, if desired) portion of the diaphragm 16.
  • the sensitivity of the sensor 10 may be somewhat reduced since a differential electrical measurement is not provided.
  • this embodiment provides for a much smaller sensor die 12 (and sensor 10) and simplified electrical connections.
  • a bond frame 70 is located on the sensor die 12 and forms an enclosure around the underside of the diaphragm 16.
  • the bond frame 70 extends around the perimeter of the sensor die 12, and also includes a bulkhead 72 extending laterally across the sensor die 12.
  • the bulkhead 72 provides environmental isolation of the contacts 50, 52, 60.
  • the chamber may operate at 600 psig or higher and the pressure fluctuations of interest can be as low as 0.1 psig at frequencies as low as 50Hz (and as high as 1000Hz). Accordingly, it may be desired to provide some pressure relief across the bond frame 70 to provide hydrostatic balance across the diaphragm 16 and allow a thinner diaphragm 16, thereby increasing the sensitivity of the sensor 10.
  • a small opening 74 is formed in the substrate 14 and below the bond frame 70 to allow pressure equalization across the diaphragm 16 to provide hydrostatic balance.
  • the opening 74 is relatively small (i.e., having a cross sectional area of a few tenths of a millimeter or less) such that any pressure fluctuations on the upper side of the diaphragm 16 are damped or attenuated as they travel through the opening 74.
  • A/C fluctuations are not transmitted to the lower side of the diaphragm 16, and only lower frequency, static or large scale pressure fluctuations pass through the opening 74.
  • the opening 74 forms a low pass frequency filter.
  • other methods for providing hydrostatic balance may be provided.
  • the bulkhead 72 provides a sealed cavity 76 ( Fig. 3 ) around the contacts 50, 52, 60.
  • the sealed cavity 76 is formed by the bond frame 70 and bulkhead 72 around the perimeter thereof, the sensor die 12 on the top side and the substrate on the bottom side 14 (see Fig. 1 ).
  • the sealed cavity 76 isolates the electrical portion of the device (i.e., the contacts 50, 52, 60) from the pressure portion (i.e., the diaphragm 16) to ensure that the pressure medium does not invade and contaminate/corrode the electrical elements or components, and also protects the electrical elements and components from high pressures.
  • each lead 56, 58 electrically connects to a contact 50, 52, and/or each contact 50, 52 is electrically connected to a pin 22, at a connection location 57, and the connection location(s) are located in the sealed cavity 76 to provide protection.
  • Each lead 56, 58 may pass under, over or through the bulkhead 72 using well known surface micromachining methods to enter the sealed cavity 76 without compromising the isolation of the sealed cavity 76.
  • Each contact 50, 52 and each pin 22 may be electrically isolated from the bond frame 70.
  • each lead 56, 58 passes under or through the bulkhead 72, each lead 56, 58 is positioned directly between the frame 70, bulkhead 72 and the body of the sensor die 12. At this point an electrically insulating material may be positioned between each lead 56, 58 and the metal layers of the bulkhead 72 to electrically isolate those component and to prevent the leads 56, 58 from shorting to the frame 70 or bulkhead 72.
  • the bulkhead 72 (and indeed the entire frame 70) is positioned on top of the dielectric layer 42, and in this case the dielectric layer 42 electrically isolates the leads 56, 58 from the bulkhead 72.
  • Fig. 7A illustrates an example sensor die 12 that does not include the bulkhead 72.
  • This example and any other examples shown herein may include the bulkhead 72.
  • the bond frame 70 forms a generally serpentine path 78 to allow pressure equalization across the diaphragm 16 as shown by the arrows of Fig. 7A .
  • the body of the sensor die 12 may also have a matching serpentine cavity 80 formed therein.
  • the opening 74 i.e., of Fig. 1
  • the serpentine cavity 78 may provide greater attenuation of the pressure fluctuations on the underside of the membrane 16, depending upon the frequency of the fluctuations.
  • the example shown in Fig. 7A may utilize a bulkhead 72 to form a sealed cavity 76 around the contacts 50, 52, 60.
  • a relatively small opening 82 may be formed in the bond frame 70 (i.e. along end wall 70') to allow pressure equalization.
  • the bond frame 70 is reflowed during the manufacturing/assembly process. Accordingly, certain channels or other flow control measures (such as placing a void in the dielectric layer 48) may be utilized to ensure that the opening 82 remains open and is not sealed by reflowed material.
  • the sensor die 12 need not necessarily include any channels or paths to provide pressure equalization, and in this case the two sides of the diaphragm 16 may be fluidly isolated from each other. It should be further understood that any of the various structures for providing pressure balance (i.e. the opening 74 formed in the substrate 14; the opening 82 formed in the bond frame 70; or the serpentine channel 78) can be used in any of the embodiments disclosed herein, or, alternately, no pressure balance structure may be provided.
  • Figs. 8-17 One process for forming the sensor die(s) 12 of Figs. 1-7 is shown in Figs. 8-17 and described below, although it should be understood that different steps may be used in the process, or an entirely different process may be used without departing from the scope of the invention. Thus, the manufacturing steps illustrated here are only one manner in which the sensor die 12 may be manufactured, and the order and details of each step described herein may vary, or other steps may be used or substituted with other steps that are well known in the art. A number of sensor dies 12 may be simultaneously formed on a single wafer, or on a number of wafers, in a batch manufacturing process. However, for clarity of illustration, Figs. 8-17 illustrate only a single sensor die 12 being formed.
  • a layer or component when a layer or component is referred to as being located “on” or “above” another layer, component or substrate, this layer or component may not necessarily be located directly on the other layer, component or substrate, and intervening layers, components, or materials could be present. Furthermore, when a layer or component is referred to as being located “on” or “above” another layer, component or substrate, that layer or component may either fully or partially cover the other layer, component or substrate.
  • Figs. 8-17 represent a schematic cross-section of the wafer during manufacturing, and the location of certain components may not necessarily correspond to a true cross section.
  • the process begins with the SOI wafer 30, such as a double sided, polished 3 inch or 4 inch (or larger) diameter wafer.
  • the device layer 34 of the wafer 30 is silicon and is about 30 microns thick (8 microns thick in another embodiment), although the device layer 34 may have a variety of thicknesses from about 1 micron to about 60 microns, or from about 3 microns to about 60 microns, or from about 3 microns to about 300 hundred microns, about or less than about 60 microns, or less than about 300 microns, or less than about 200 microns or greater than about 1 micron, or greater than about 3 microns, or have other thicknesses as desired (it should be understood that the thickness of the various layers shown in the drawings are not necessarily to scale).
  • the device layer 34 may be doped (either n-doped or p-doped) silicon and may have a (111) crystal orientation to aid in subsequent deposition of the piezoelectric film 42. If desired, the device layer 34 can be made of other materials besides silicon, such as sapphire, gallium nitride, silicon nitride, silicon carbide, or high temperature-resistant materials or ceramics. Although the device layer 34 may be made of silicon carbide, in one embodiment of the present invention the device layer 34 is made of non-silicon carbide semiconductor materials.
  • the responsiveness of the sensor die 12 to a range of pressure fluctuations is directly related to the thickness of the diaphragm 16.
  • the thickness of the device layer 34 will ultimately determine the thickness of the diaphragm 16, and thus the thickness of the device layer 34 should be carefully selected.
  • the thickness of the device layer 34 could be reduced during later processing steps to tailor the responsiveness of the diaphragm 16 to pressure ranges and fluctuations of interest.
  • the base layer 32 may also be made of silicon or other materials listed above, and can have a variety of thicknesses, such as between about 100 microns and about 1,000 microns, or greater than 1000 microns, and more particularly, about 500 microns.
  • the base layer 32 should be of sufficient thickness to provide structural support to the sensor die 12.
  • the base layer 32 is single crystal silicon having a (100) crystal orientation to allow easy etching thereof.
  • the insulating layer 36 can be of any variety of materials, and is typically silicon dioxide.
  • the insulating layer 36 acts as an etch stop, and also provides electrical isolation to the wafer 30.
  • the insulating layer 36 may have a variety of thicknesses, such as between about 0.5 microns and about 4 microns, and is typically about 1 or 2 microns thick.
  • a lower insulating layer 84 (such as a 0.3 micron thick layer of silicon dioxide) may be deposited or grown on the wafer 30.
  • the lower insulating layer 84 may have the same properties as the insulating layer 36. Alternately, the lower insulating layer 84 may be deposited or grown after the piezoelectric film 42 is deposited, as described below and shown in Fig. 9 .
  • the piezoelectric film 42 is deposited on top of the device layer 34.
  • the piezoelectric film 42 may coat all of the device layer 34. Alternately, the piezoelectric film 42 may cover only part of the device layer 34 (i.e. only the diaphragm 16, or only where the electrodes 44, 46 will be located).
  • the material of the piezoelectric film 42 is selected based on its operating temperature range, electrical resistivity, piezoelectric coefficient, and coupling coefficient. Aluminum nitride remains piezoactive up to 1,100°C, and thus may be useful for the piezoelectric film.
  • gallium nitride gallium orthophosphate (GaPO4), lanthanum titanate (which can take the form of La 2 Ti 2 O 7 ) or langasite (which can take the form of several compositions, typically including lanthanum and gallium, such as La 3 GasSiO 14 , La 3 Ga 5.5 Ta 0.5 O 14 , or La 3 Ga 5.5 Nb 0.5 O 14 ) may be used.
  • any other piezoelectric material may be utilized as the film 42, depending upon the operating temperature.
  • the piezoelectric film 42 can be deposited using metal organic chemical vapor deposition ("MOCVD”), molecular beam epitaxy (“MBE”), vapor phase epitaxy (“VPE”) or any other deposition process which can provide epitaxial growth of the piezoelectric film 42. Further alternately, the piezoelectric film 42 can be sputter deposited in either nanocrystalline or amorphous form.
  • MOCVD metal organic chemical vapor deposition
  • MBE molecular beam epitaxy
  • VPE vapor phase epitaxy
  • the piezoelectric film 42 can be sputter deposited in either nanocrystalline or amorphous form.
  • the device layer 34 need not necessarily be of (111) silicon, and instead a thin film of metal, such as platinum, may be deposited on the device layer 34 prior to deposition of the piezoelectric film 42 to act as an electrode during the piezoelectric film sputtering process. If the metal electrode is utilized during the sputtering process, the device layer 34 need not necessarily be doped, as the metal film could instead provide the desired electrical conductivity to the device layer 34.
  • the piezoelectric film 42 can have a variety of thicknesses, such as between about 0.2 and about 2 microns.
  • part of the piezoelectric film 42 is then patterned and removed at 86 to expose part of the device layer 34 therebelow.
  • the piezoelectric film 42 can be etched/patterned by any acceptable method, such as a high density plasma etching (i.e. inductively coupled plasma ("ICP") etching).
  • ICP inductively coupled plasma
  • a metallization layer 88 is then selectively deposited, such as by sputtering and photo patterning, to form or contribute materials to the center electrode 44, outer electrode 46, leads 56, 58 (not shown in Fig. 11 ), reference contact 60, output contacts 50, 52 and bond frame 70.
  • the metallization layer 88 provides good ohmic contact to the active layer 34 and also operates as a diffusion barrier, as will be described in greater detail below.
  • the metallization layer 88 includes a layer of tantalum located on the wafer 30, with a layer of tantalum silicide located on the tantalum layer, and a layer of platinum located on the tantalum silicide layer.
  • the center electrode 44, outer electrode 46, reference contact 60, output contacts 50, 52 and leads 56, 58 can have a variety of shapes and sizes.
  • the center electrode 44 has dimensions of about 3900 x 3900 microns
  • the outer electrode 46 has outer dimensions of about 6000 x 6000 microns
  • the reference contact 60 has dimensions of about 2000 x 1000 microns
  • each output contact 50, 52 has dimensions of about 600 x 600 microns
  • each lead 56, 58 has a width of between about 50 and about 150 microns.
  • the passivation layer 48 is then deposited on the wafer 30 and over the metallization layers 88 and piezoelectric film 42.
  • the passivation layer 48 is SiO x N y and is deposited by plasma enhanced chemical vapor deposition ("PECVD") to a thickness of about 1 micron (0.3 microns in another embodiment).
  • PECVD plasma enhanced chemical vapor deposition
  • the passivation layer 48 can be made of any of a wide variety of protective/insulating materials. As noted above the passivation layer 48 may be omitted if the additional protection/insulation is not needed. However, for the remainder of this process flow it is assumed the passivation layer 48 is utilized.
  • portions of the passivation layer 48 are then removed to expose the metallization portion 88 of the reference contact 60, output contacts 50, 52 and bond frame 70.
  • the metallization layer 88 forming the electrodes 44, 46 and leads 56, 58 remains buried.
  • a bonding material 90 is deposited on the exposed metallization layers 88 to add further structure to the contacts 50, 52, 60 and bond frame 70.
  • the materials for, and deposition of, the bonding materials 90 will be described in greater detail below, but in one embodiment includes gold and germanium.
  • the lower insulating layer 84 is then patterned to expose portions of the base layer 32 for etching.
  • the exposed portions of the base layer 32 are removed to define a cavity 92, above which is located the diaphragm 16, and to define a pair of dicing lanes 94.
  • the portions of the oxide layer 36 located under the diaphragm 16 may also be removed to reduce thermal stresses on the diaphragm 16.
  • the diaphragm 16 can have a variety of sizes, and in one embodiment has a surface area of between about 0.25 mm 2 and about 4 mm 2 . This etch step of Fig.
  • DRIE deep reactive ion etching
  • a wet etch such as a KOH etch
  • KOH etch any of a variety of other etching methods.
  • the sensor die 12 is then singulated along the dicing lanes 94, resulting in the final structure shown in Fig. 17 .
  • Figs. 18 and 19 illustrate the deposition of the metallization layer 88 directly on the device layer 34 (i.e. when forming the reference contact 60).
  • the metallization layer includes a first layer or adhesion layer 102, a second layer or outward diffusion blocking layer 104, and a third layer or inward diffusion blocking layer 106.
  • the adhesion layer 102 can be made of any of a variety of materials which adhere well to the wafer 30 (i.e. silicon). Thus, the material of the adhesion layer 102 can vary depending upon the material of the wafer 30, although the adhesion layer 102 is primarily selected based on its ability to bond strongly to the wafer 30.
  • Tantalum is one example of the adhesion layer 102 because tantalum adheres well to a variety of materials. However, besides tantalum, various other materials such as chromium, zirconium, hafnium, or any element which reacts favorably with the wafer 30 and forms compounds which bond strongly to the wafer 30 may be utilized as the adhesion layer 102.
  • the adhesion layer 102 can have a variety of thicknesses, and can be deposited in a variety of manners. However, the adhesion layer 102 should have sufficient thickness to ensure proper adhesion to the wafer 30, but should not be so thick so as to add significant bulk to the metallization layer 88.
  • the adhesion layer 102 may be initially deposited to a thickness of between about 100 Angstroms and about 10,000 Angstroms, and may be deposited by plasma enhanced physical vapor deposition or other suitable deposition techniques known in the art.
  • the presence of oxygen at the interface of the adhesion layer 102 and the wafer 30 can inhibit silicide formation which material is desired for its diffusion blocking properties.
  • the presence of oxygen at the interface can also cause adverse metallurgical transformations in the adhesion layer 102 to thereby create a highly stressed (i.e., weak) adhesion layer 102.
  • the upper surface of the device layer 34 may be cleaned to remove oxides.
  • This cleaning step may involve the removal of oxides through plasma sputter etching, or a liquid HF (hydrofluoric acid) solution or a dry HF vapor cleaning process or other methods known in the art.
  • the adhesion layer 102 should be deposited on the device layer 34 shortly after the cleaning step to ensure deposition thereon before oxides have the opportunity to redevelop on the device layer 34 (i.e. due to oxidizing chemical reactions with oxygen in the surrounding environment).
  • Outwardly diffusing materials may react with the materials of the metallization layer 88 which can weaken the metallization layer 88.
  • the second layer 104 is made of a material or materials which blocks the outward diffusion of the material of the wafer 30.
  • the second 104 and third 106 layers are designated as inward and outward diffusion blocking layers, respectively, it should be understood that the second 104 and third 106 layers may not, by themselves, necessarily block diffusion in the desired manner. Instead, each of the layers 104, 106 may include or contribute a material which reacts to form a diffusion blocking layer upon sintering, annealing, chemical reactions, etc. of the metallization layer 88, as will be described in greater detail below.
  • the second layer 104 can be made of any of a wide variety of materials depending upon the materials of the wafer 30 (the outward diffusion of which is desired to be blocked).
  • the second layer 104 is tantalum silicide although a variety of other materials including but not limited to tantalum carbide and tungsten nitride may be utilized.
  • the second layer 104 should have a thickness sufficient to prevent outward diffusion of the wafer material 30, or to contribute sufficient materials to form a sufficient outward diffusion barrier layer after annealing.
  • the second layer 104 may be initially deposited to a thickness of between about 100 Angstroms and about 10,000 Angstroms by plasma sputtering, or other suitable deposition techniques known in the art.
  • the tantalum silicide may be deposited directly in its form as tantalum silicide.
  • layers of tantalum and layers of silicon may be deposited such that the layers subsequently react to form the desired tantalum silicide.
  • alternating, thin (i.e. 5 to 20 Angstroms) discrete layers of the two basic materials (tantalum and silicon) are deposited on the adhesion layer 102 in a co-deposition process.
  • the number of alternating layers is not critical provided that the total thickness of the composite layer is between about 100 and about 10,000 Angstroms as described above.
  • the alternating layers of tantalum and silicon are deposited, the alternating layers are exposed to elevated temperatures during an annealing step, which is discussed in greater detail below. During the annealing step the alternating layers of tantalum and silicon diffuse or react to form a single layer of tantalum silicide.
  • the relative thickness of the deposited layers of tantalum and silicon during the co-deposition process controls the ratio of tantalum and silicon in the resultant tantalum silicide layer 104.
  • the ability to control the relative thickness of the tantalum and silicon layers allows a silicon-rich or silicon-lean layer of tantalum silicide to be formed.
  • a relatively silicon-rich layer of tantalum silicide i.e. tantalum silicide having an atomic composition of a few percentage points richer in silicon than stoichiometric tantalum silicide (TaSi 2 )
  • TaSi 2 stoichiometric tantalum silicide
  • the third layer 106 of the metallization layer 88 is made of a material or materials that block or limit inward diffusion of undesired elements, compounds or gases.
  • the third layer can be made of materials which block the inward diffusion of gases such as nitrogen, oxygen or carbon dioxide in the surrounding environment, or which block the inward diffusion of solid elements or compounds located on the metallization layer 88. These undesired elements, compounds or gases can adversely react with the other materials of the metallization layer 88 or the materials of wafer 30.
  • the third layer 106 may be made of a variety of materials, such as platinum, although the materials of the third layer depends upon the materials of the wafer 30 and the materials of the adhesion 102 and second layer 104, as well as the elements, compounds or gases which are desired to be blocked from diffusing inwardly.
  • the third layer 106 can be deposited to an initial thickness of between about 100 Angstroms and about 10,000 Angstroms by plasma sputtering or other suitable deposition methods known to those skilled in the art.
  • the first layer 102 includes a tantalum layer having a thickness of about 1500 Angstroms
  • the second layer 104 includes tantalum silicide having a thickness of about 3000 Angstroms
  • the third layer 106 is platinum having a thickness of about 10,000 Angstroms.
  • the specific thickness tolerances of the various layer 102, 104, 106 is determined by the need to create an effective adhesion layer and for the processed materials to diffuse and create effective inward and outward diffusion barriers, while leaving enough platinum available on the outer surface of the metallization layer 88 for platinum-platinum wire bonding.
  • Fig. 18 illustrates the metallization layer 88 after deposition of the first layer 102 (tantalum in the illustrated embodiment), second layer 104 (tantalum silicide in the illustrated embodiment) and third layer 106 (platinum in the illustrated embodiment).
  • the metallization layer 88 is annealed (also termed sintering) to cause certain reactions and/or reaction byproducts.
  • the structure shown in Fig. 18 is annealed for about 30 minutes at about 600°C in a vacuum. The annealing process is carried out such that the layer of tantalum silicide 104 is formed (if tantalum and silicide are deposited as alternating layers) or until the other desired reactions are complete.
  • a two step anneal process may be utilized.
  • the two step anneal process includes ramping to a temperature of about 450°C by increasing temperature (from room temperature) about 6°C - 10°C per minute.
  • the first anneal step is then performed by holding the temperature at about 450°C for about 1 hour.
  • the temperature is slowly increased to about 600°C over a period of about 15 minutes, and then the temperature is held at about 600°C for about 1 hour for the second anneal step.
  • the metallization layer 88 is then allowed to slowly cool.
  • the two step anneal process improves adhesion of the metallization layer 88 to the wafer 30 and in particular improves adhesion of the adhesion layer 102/108 to the piezoelectric film 42 ( Fig. 20 ).
  • a significant portion of the two step anneal process occurs at a relatively low temperature (i.e., below 600°C)
  • diffusion of platinum or tantalum through the piezoelectric film 42 and into the device layer 34 is reduced, thereby reducing electrical leakage issues.
  • Fig. 19 illustrates the structure of Fig. 18 after the anneal step.
  • the first, second and third layers may be referred to herein as the "tantalum layer 102," “tantalum silicide layer 104" and “platinum layer 106,” respectively.
  • this convention is included for ease of discussion purposes only and is not intended to convey that the layers 102, 104, 106 are limited to those particular materials.
  • various layers or materials other than those shown in Fig. 19 and discussed below may form in the metallization layer 88 after annealing, and Fig. 19 merely illustrates the presence of the various, major layers which are expected to be present after annealing.
  • the wafer 30 is a SOI wafer and the first 102, second 104 and third 106 layers are tantalum, tantalum silicide and platinum, respectively, after annealing an inner tantalum silicide layer 108 is formed as a reaction product of the adhesion layer 102 and the wafer 30.
  • the inner tantalum silicide layer 108 adheres well to the tantalum adhesion layer 102 and to the wafer 30, and therefore provides a high adhesion strength for the metallization layer 88.
  • tantalum silicide generally blocks the outward diffusion of many materials (including silicon)
  • the inner tantalum silicide layer 108 also acts as an outward diffusion-blocking layer for the silicon wafer 30.
  • various other diffusion-blocking tantalum compounds may be formed depending upon the material of the wafer 30.
  • the upper platinum layer 106 is converted to a layer of platinum silicide 110 due to reactions between the platinum of layer 106 and the silicon of the wafer 30 and/or the silicon of the tantalum silicide 104.
  • the resultant platinum silicide 110 acts as an inward diffusion-blocking layer, and in particular blocks the inward diffusion of oxygen and nitrogen.
  • the platinum silicide layer 110 may not be entirely platinum silicide, and may instead include a gradient of platinum and platinum silicide such that the upper surface of the metallization layer 88 is at least about 90%, or at least about 99%, or at least about 99.99% platinum.
  • tantalum silicide i.e., having a thickness of about 500 angstroms or other thickness as desired
  • tantalum nitride i.e., having a thickness of about 500 angstroms or other thickness as desired
  • tantalum silicide When tantalum silicide is used as the second layer 104 of the metallization layer 88, the tantalum silicide effectively prevents oxygen from diffusing therethrough to form an oxide at the silicon/tantalum interface. However, at temperatures above about 700°C, silicon may diffuse upwardly through the metallization layer 88 to form a silicon oxide layer on top of the metallization layer 88, which makes subsequent bonding of wires thereto difficult.
  • tantalum nitride when tantalum nitride is utilized as the second layer 104, the tantalum nitride not only prevents oxygen from diffusing inwardly, but also prevents silicon from diffusing outwardly to protect the top surface of the metallization layer 88. It is believed that the diffusion barrier effectiveness of tantalum base liners increases with higher nitrogen content, at least up to an N to Ta stoichiometry of 1:1. Thus, if desired, tantalum nitride can also be used as the second layer 104.
  • Fig. 19 illustrates the post-annealing metallization layer 88 located directly on the device layer 34 to form at least part of the reference contact 60.
  • metallization layers 88 are also positioned on top of the piezoelectric film 42 (i.e. to form the electrodes 44, 46, contacts 50, 52, leads 56, 58 and part of the bond frame 70).
  • the metallization film 88 deposited on the piezoelectric film 42 in Fig. 11 can have the same structure and be deposited in the same manner as the metallization film 88 of Fig. 18 and described above.
  • the post-annealing structure of the metallization film 88 located on the piezoelectric film 42 shown in Fig.
  • the metallization layer 88 provides contacts 50, 52, 60, electrodes 44, 46, and leads 56, 58 and a bond frame 70 that are metallurgically stable at high temperatures and resist diffusion and chemical reactions.
  • the bonding layer 90 includes first 120 and second 122 bonding materials or layers that can form eutectics with each other.
  • the first bonding material 120 can be gold, or any other element or material that can form a eutectic alloy with the second bonding material 122.
  • the second bonding material 122 may be germanium, tin, or silicon, or any element or material that can form a eutectic alloy with the first bonding material 120.
  • Representative examples of other materials of the bonding layer 90 includes InCuAu, AuNi, TiCuNi, AgCu, AgCuZn, InCuAg, and AgCuSn.
  • Both the first 120 and second 122 bonding materials may be deposited on the associated metallization layer 88 by plasma sputtering or other suitable deposition techniques known to those skilled in the art. Further, the first 120 and second 122 bonding materials can be deposited in a variety of thicknesses. However, the thickness of the bonding materials 120, 122 should be selected to provide the desired ratio between the first 120 and second 122 bonding materials in the end product bond.
  • the bonding layer 90 includes a capping layer 124 located on the second bonding material 122.
  • the capping layer 124 caps and protects the second bonding material 122 to prevent oxidation of the second bonding material 122.
  • the capping layer 124 can be any of a wide variety of materials which resist oxidation, such as gold.
  • the capping layer 124 can be the same material as the first bonding layer 120 so that the capping layer 124 participates in the eutectic joining process.
  • the capping layer 124 may be quite thin, such as about 1000 Angstroms or less.
  • the sensor die 12 is then desired to be coupled to the substrate 14. As shown in Fig. 22 , the sensor die 12 is inverted from its position shown in Fig. 17 and aligned with the substrate 14.
  • the substrate 14 has the metallization layer 88 and bonding material 90 deposited thereon in generally the same manner as described above in the context of the sensor die 12.
  • the substrate 14 may be made of different materials than the sensor die 12, some of the materials of the metallization layer 88 on the substrate 14 may differ from those described above in the context of the sensor die 12.
  • the layer 108 of the metallization layer 88 may be or include materials other than tantalum silicide, such as tantalum nitride, tantalum aluminide or ternary compounds of tantalum, aluminum, and nitrogen.
  • the material of the adhesion layer 102 of the metallization layer 88 can vary depending upon the materials of the substrate 14.
  • the second bonding materials 122 of the bonding materials 90 are germanium, and that the first bonding materials 120 and capping materials 124 are gold to allow discussion of the specific properties of the gold/germanium eutectic alloy.
  • this discussion is for illustrative purposes and it should be understood that various other materials may be utilized as the first bonding materials 120, second bonding materials 122, and capping materials 124.
  • the substrate 14 and sensor die 12 are aligned as shown in Fig. 22 in preparation of bonding, and either or both components may include self alignment features to aid in the alignment process.
  • the metallization layers 88/bonding layers 90 of the substrate 14 have a pattern matching the pattern of the metallization layers 88/bonding layers 90 of the sensor die 12 such that, once joined, those materials match up to form/complete the electrical contacts 50, 52, 60 and the bond frame 70 joining those components together.
  • the sensor die 12 and substrate 14 are pressed together such that their bonding layers 90 contact each other, as shown in Figs. 23 and 24 .
  • the materials of the bonding layers 90 should be sufficiently flat such that during the eutectic bonding process (described below) the liquids formed during the bonding process fully fill any voids or gaps between the bonding layers 90.
  • the sensor die 12 and substrate 14 are next joined or bonded in a transient liquid phase bonding process which is well known in the art, but is outlined briefly below.
  • a light pressure e.g. a few pounds
  • the bonding layers 90 are then exposed to a temperature at or above the eutectic point or eutectic temperature of the bonding alloy, i.e. a gold/germanium alloy.
  • the eutectic temperature of a gold/germanium alloy is about 361°C.
  • the bonding layers 90 are exposed to a temperature of about 450°C.
  • the actual bonding temperatures will depend upon the diffusion rate of the bonding materials 90, the thickness of the bonding materials 90 and the time available to complete the diffusion such that a uniform solid solution of the bonding alloy is achieved.
  • zones of melted or liquid materials 132 are formed at each interface (see Fig. 25 ) due to the melting of materials.
  • the entire capping layers 124 have melted (due to the thinness of those layers) to form the central liquid zone 130, and portions of the second bonding layers 122 and first bonding layers 120 have melted to form the top and bottom liquid zones 132.
  • Each zone of liquid material 130, 132 has a composition that is at or near the eutectic composition.
  • the liquid zones 130, 132 continue to grow and expand until all the material of the germanium layers 122 melt and dissolve into the liquid zones 130, 132.
  • the separate liquid zones of Fig. 25 grow and ultimately combine to form a single larger liquid zone 134 ( Fig. 26 ).
  • the last of the material of the germanium layers 122 have been dissolved, and the liquid zone remains at composition A of Fig. 32 .
  • the materials of the gold layers 120 adjacent to the liquid zone 134 continue to liquefy as the surrounding materials approach the ambient temperature.
  • the germanium in the liquid zone 134 is diluted and the percentage of germanium in the liquid zone 134 is thereby reduced.
  • the composition of the liquid zone 134 moves up and to the left of point A along the liquidus line 138 of Fig. 32 .
  • the liquid composition ultimately reaches the composition at point B of Fig. 32 when the liquid zone 134 reaches the ambient temperature of 450°C.
  • Fig. 27 illustrates the bonding process wherein the liquid zone 134 has grown and added gold such that the liquid zone is at composition B. At this stage the liquid zone 134 has reached the ambient temperature of 450°C, and has a composition of about twenty four atomic percent germanium and seventy six atomic percent gold.
  • the germanium in the liquid zone 134 begins diffusing into the remaining solid gold layer 120 at the interface of the liquid zone 134 and the gold layers 122. As this occurs, the concentration of germanium in the liquid zone 134 adjacent to the interface drops. Once the percentage of germanium at the interface drops sufficiently low (i.e., about three atomic percent germanium or less), the liquid zone at the interface forms into a solid solution phase 140 (see Fig. 28 ).
  • the newly-formed solids 140 have a composition indicated at point C on the graph of Fig. 32 . As can be seen in Fig. 32 , the point C is located on the solidus line 142, which indicates the percentage of germanium at which solids will form for a given temperature. Thus the newly-formed solids have about three atomic percent germanium and about ninety-seven atomic percent gold.
  • the ambient temperature continues to be held at 450°C and remaining germanium in the liquid zone 134 continues to diffuse outwardly, through the newly-formed solids 140 and into the predominantly gold layers 120.
  • the solids 140 grow inwardly until the entire liquid zone 134 is consumed ( Fig. 29 ).
  • the solid 140 may be relatively germanium-rich (i.e., about three atomic percent germanium) and the surrounding gold layers 120 may be relatively germanium-poor (i.e. less than about three atomic percent germanium).
  • the germanium continues to diffuse, through solid-state diffusion, from the solid 140 into the gold layers 120 until equilibrium is reached and both the solid 140 and the gold layers 120 all have the same composition (shown as solid 140 in Fig. 30 ).
  • the solid 140 formed after solid state diffusion is a gold/germanium alloy or solid solution alloy having a composition of about three atomic percent germanium.
  • the amount of available germanium may be limited by restricting the thickness of the germanium layer 122 to a relatively low percentage relative to the available gold.
  • the amount of available germanium can also be reduced by scavenging (with a germanium scavenging material such as platinum, nickel and chromium) so that the resultant solid 140 has a composition of less than about three atomic percent germanium (e.g., as low as about 0.5 atomic percent germanium or even lower). In either case, when the amount of germanium is restricted/reduced, the composition of the solid 140 is located to the left of point C of Fig. 32 .
  • reducing the atomic percentage of germanium to lower than three atomic percent provides a solution located on the solidus line 142 above and to the left of point C. Moving the composition to the left of point C provides a solid solution with a melting point above 450°C, up to a theoretical maximum of 1064°C.
  • the transient liquid phase bonding method described above allows the joining of the silicon sensor die 12 and the ceramic substrate 14 at a relatively low temperature (but above the eutectic temperature) which avoids damaging any temperature-sensitive components, yet results in a bond having a relatively high melting temperature.
  • the resultant bonding material 140 is a hypoeutectic gold-germanium solid alloy having a relatively high melting temperature.
  • the solid bonding material 140 can also be a hypoeutectic gold-silicon solid alloy or a hypoeutectic gold-tin solid alloy depending upon the starting materials for the bonding layers 90.
  • the bonding process can also be performed using a eutectic die bonder with heated stage and ultrasonic energy for acceleration of the fusion process.
  • Fig. 31 illustrates part of the sensor die 12 and substrate 14 after the bonding layers 90 have been joined to form a single bonded layer 140.
  • Fig. 31 illustrates the circled area "23" indicated in Fig. 22 , after bonding.
  • the metallization film 88 includes the inward diffusion blocking layer 110 which blocks inward diffusion of materials into or through the metallization film 88 during the bonding process.
  • layers 104 and/or 102 and/or 108 block outward diffusion of materials of the sensor die 12 and/or substrate 14 during bonding.
  • the metallization layer 88 resists diffusion therethrough, adheres well to various substrates, and is thermodynamically stable, even at elevated temperatures for extended periods of time.
  • the metallization layer 88 and bonding materials 90 allow low temperature bonding with robust high temperature operation.
  • the substrate 14 is positioned inside and coupled to the ring 18, and that attachment process is now described in greater detail and shown in Figs. 33-35 .
  • the attachment of the substrate 14 and ring 18 are now described (after the attachment of the sensor die 12 and substrate 14 was described above), during actual assembly the order of operations may be reversed. More particularly, during assembly the substrate 14 may first be attached to the ring 18, and the sensor die 12 then attached to the substrate 14/ring 18 assembly. This order of operations ensures that the more sensitive electrical components of the sensor die 12 are not exposed to high temperatures when the substrate 14 is brazed to the ring 18.
  • the substrate 14 may be made of a material which can withstand relatively high temperatures, resists oxidation, and has a thermal coefficient of expansion that matches that of the sensor die 12 relatively well.
  • the substrate 14 can be made of a variety of ceramic materials, such as monolithic silicon nitride, aluminum oxide or aluminum nitride (hot-pressed and sintered (i.e. polycrystalline aluminum nitride)).
  • the ring 18 may be made of a material which can withstand relatively high temperatures, resists oxidation, and has a thermal coefficient of expansion that matches that of the substrate 14 relatively well.
  • the ring 18 can be made of a variety of metal alloys such as THERMO-SPAN® metal alloy, sold by CRS Holdings, Inc. of Wilmington, Delaware, or other metals with similar environmental resistance and physical properties.
  • the joining technique should be carefully selected, especially when the joint will be exposed to elevated temperatures and a wide temperature range.
  • Brazing may be utilized to join the ceramic substrate 14 to the metal ring 18, in which case the substrate 14 will first need to be treated with a material, such as a thin film metallization, to aid in the brazing process.
  • Fig. 33 illustrates the post-annealing metallization layer 88, including sublayers 102, 104, 108, 110 located on the end surface of the substrate 14.
  • the metallization layer 88 of the substrate 14 is located on its circumferential outer surface 146.
  • a thin layer of nickel i.e. 10 microns may be deposited on the brazing (inner) surface of ring 18.
  • a cylindrical magnetron plasma sputter deposition system may be utilized.
  • the substrate 14 is placed on a rotating fixture inside the sputter chamber of the cylindrical magnetron.
  • the cylindrical magnetron progressively deposits the first layer 102, the second layer 104 and the third layer 108 onto the outer surface 146 of the substrate in a direction normal to the outer surface 146. In this manner the cylindrical magnetron provides a sputtering flux that is normal to the curved surface (i.e.
  • cylindrical sputtering may be easier and more effective, but special fixtures and tools may be used in a conventional deposition system to obtain the same results and thus systems other than cylindrical sputtering may be used.
  • the first 102, second 104 and third 106 layers may be made of the materials described above and deposited in the manner described above in the context of Figs. 18-20 .
  • the pre-annealing metallization layer 88 on the outer surface 146 includes a tantalum layer 102 having a thickness of about 500 Angstroms; a silicon-rich tantalum silicide layer 104 having a thickness of about 5000 Angstroms; and a platinum layer 106 having a thickness of about 3000 Angstroms.
  • the layers 102, 104, 106 are annealed to provide the layers 108, 102, 104, 110 shown in Figs. 19 and 33 .
  • the annealing step may be omitted as the subsequent brazing process described below may drive the same reactions.
  • Fig. 33 illustrates the substrate 14 spaced away from the ring 18, and Fig. 34 illustrates the substrate 14 loosely fit into the ring 18.
  • a ductile braze material, braze slurry, braze alloy or braze paste 150 is deposited near or around the outer circumference of the substrate 14 and in intimate contact with the ring 18 and the metallization layer 88.
  • the braze material 150 is applied to the outer diameter of the substrate 14 and/or the inner diameter of the ring 18.
  • braze material 150 depends upon the type of materials of the substrate 14 and ring 18 but can be any high temperature braze material 150 that can withstand high temperatures and corrosive environments, such as a gold/nickel braze material.
  • the braze material 150 may be deposited at room temperature and then exposed to an elevated temperature (e.g. about 980°C for a gold/nickel braze) suitable to melt the braze material 150.
  • the melted braze material 150 is drawn into the gap between the substrate 14 and the ring 18 by capillary action (shown in Fig. 35 ).
  • the outer edges of the substrate 14 may be chamfered (not shown) to provide an exposed area of the metallization 88 and to "funnel" the braze material 150 into the gap between the substrate 14 and the ring 18.
  • the temperature is then reduced such that the braze material 150 cools and forms a strong bond in the well-known manner of standard brazing.
  • Fig. 35 illustrates the sensor die 12 positioned above the completed brazed ring 18/substrate 12 assembly for subsequent joining in the process described above and shown in Figs. 22-31 .
  • the substrate 14 and the ring 18 may be sized to form a mechanically robust joint.
  • the ring 18 may expand to relatively loosely receive the substrate 14 therein (shown in Figs. 33 and 34 ). Because the ring 18 is metal, the ring 18 has a relatively large coefficient of thermal expansion relative to the substrate 14. Upon cooling, the metal ring 18 contracts around the substrate 14, thereby placing the substrate 14 in a state of radial compression which provides a more robust structure.
  • the sensor die 12 includes a plurality of contacts (three contacts 50, 52 and 60 in the embodiment shown in Fig. 3 ).
  • Pins 22 (only one of which is shown in Fig. 1 ) are electrically coupled to each of the contacts 50, 52 or 60 to provide an output of the sensor die 12 to an external controller, processor, amplifier or the like.
  • the pins 22 can be made of any of a variety of materials, such as an oxidation resistant metal which forms a tenacious oxide film and resists exfoliation due to expansion of the oxide.
  • the pins 22 can be made of nickel, stainless steel, HASTELLOY® alloys sold by Haynes International, Inc. of Kokomo, Indiana, or KOVAR® alloy sold by CRS Holdings, Inc. of Wilmington, Delaware, depending upon the desired properties such as electrical conductivity, thermal expansion coefficient, or the like.
  • the pins 22 may also take the form of a tube or other metallic component.
  • the pins 22 must be properly located in the substrate 14 so that the pins 22 align with the associated contacts 50, 52, 60 on the sensor die 12.
  • the mounting process described below may be utilized to precisely mount the pins 22 into the substrate 14, and in a manner such that the pins 22 and associated attachment structures can withstand harsh environments.
  • Figs. 36-38 which describe a process for mounting the pins 22, illustrate only a single pin 22, but it should be understood that any desired number of pins 22 can be mounted in this manner.
  • Fig. 36 illustrates the substrate 14 having a pair of opposed surfaces 154, 156, with an opening 158 extending from the first 154 to the second 156 surface and defining an attachment surface 160.
  • the substrate 14 can have a variety of thicknesses, such as between about 0.60 and about 0.006 inches, and has a thickness of about 0.060 inches in one embodiment.
  • the opening 158 takes the form of a stepped bore opening ( Fig. 37(a) ).
  • the stepped bore opening 158 can be formed by ultrasonic drilling or by other acceptable methods.
  • an active metal braze 162 is deposited on the substrate 14 adjacent to or into the opening 158 ( Fig. 37(b) ).
  • the active braze 162 is then reflowed, in a vacuum, such that the active braze 162 flows downwardly in its liquid state, coats the side walls 160 of the opening 158 and fills the smaller diameter.
  • the active braze 162 flows downwardly, it chemically reacts with the substrate 14 to allow subsequent wetting of the substrate 14.
  • the active metal braze 162 coats the side walls 160, preparing the substrate for subsequent brazing with conventional braze alloys that are the same as or similar to the braze alloys 150 described above.
  • the active metal braze 162 fills and plugs the smaller diameter portion of the opening 158.
  • the plug formed by the active metal braze material 162 provides a continuous metal on side 156 of the substrate 14 such that after grinding, lapping or other finishing methods a flat and uninterrupted metal contact, that is coplanar with the substrate 14, is provided. Accordingly, the smaller diameter of the stepped opening 158 and the materials and quantity of active metal braze 162 should be selected such that the active metal braze 162 can plug the smaller diameter portion of the opening 158.
  • the pin 22 is inserted into the larger diameter portion of the opening 158 until the pin 22 bottoms out on the active braze material 162.
  • a second braze material 164 is then introduced into the remaining volume of the larger diameter portion of the opening 158 such that the second braze material 164 surrounds the pin 22 and secures/brazes the pin 22 to the active metal braze 162/substrate 14.
  • the opposed surface of the substrate 14 is then planarized, such as by grinding and polishing, to sufficient flatness for the subsequent bonding step of the sensor die 12.
  • the substrate assembly 14 and associated metallizations are planarized to within 1 micron, or more particularly, 0.5 microns.
  • the planarization ensures that the metallization film 88 and bonding film 90 can be located thereon, and the substrate 14 can be attached to the sensor die 12.
  • the multiple braze, or "step-braze" process shown in Figs. 37(a)-37(e) can be utilized to join the pin 22 and substrate 14 wherein the active braze 162 acts as a premetallization and the second braze material 164 creates the joint.
  • the brazing materials 162, 164 can be any of a variety of braze metals which can be utilized to braze the pin 22 to the substrate 14 of interest.
  • the active metal braze 162 may be a titanium activated braze, such as titanium/copper, titanium/nickel, titanium/gold, titanium/nickel/gold, and the like.
  • the second braze material 164 can be any standard braze, or high temperature braze material, such as gold/nickel, or copper/nickel with a eutectic ratio of copper/nickel, which can withstand relatively high temperatures (i.e., up to 600-700°C) and provide corrosion resistance.
  • the metallization film 88 and bonding material 90 are deposited on the substrate 14 such that the deposited metallization film 88/bonding materials 90 are generally aligned with, or electrically coupled to, the active braze material 162.
  • the deposited metallization film 88/bonding materials 90 are electrically coupled to the pin 22 through the braze materials 162, 164.
  • the bonding material 90 of the substrate is then bonded to the sensor die 12 ( Fig. 37(g) ), as described above and shown in Figs. 22-31 , to complete electrical contact between the conductor pin(s) 22 and the contacts 50, 52, 60.
  • the metallization film 88/bonding materials 90 not only mechanically couple the sensor die 12 and substrate 14, but also electrically couple the sensor die 12 and pin 22.
  • Figs. 38(a)-(f) illustrates an alternative method for brazing the pin 22 to the substrate 14. More particularly, in this embodiment the substrate includes a non-stepped bore opening, such as a straight-walled opening 158 ( Fig. 38(a) ) or a slightly tapered opening 158 ( Fig. 38(b) ).
  • the opening 158 of Figs. 38(a) or (b) may be drilled ultrasonically, by a waterjet, laser, electronic discharge ablation, or otherwise, and may have a diameter accommodating (i.e. slightly larger than) the diameter of the pin 22.
  • the pin 22/opening 158 may have an opening of around 0.020 inches, or around 0.030 inches, or larger.
  • a waterjet may be less expensive, but may result in an opening having a slight taper as shown in Fig. 38(b) .
  • the taper is slight (i.e. less than a few thousands of an inch throughout the thickness of the substrate 12 having a thickness of about 0.060 inches, or up to 0.125 inches, or greater) the taper has no adverse effects.
  • the opening 158 of Figs. 38(a) and 38(b) can each be formed by a single step, in contrast with the stepped opening 158 of Fig. 37(a) which must be formed in two steps, and which requires greater precision.
  • forming a stepped bore requires the use of ultrasonic drilling or the like, which is more expensive than waterjet drilling which can be used in the opening(s) of Fig. 38 .
  • the active metal braze 162 is applied and reflowed in largely the same manner as described above, as shown in Figs. 38(c) and 38(d) . If the opening 158 has a taper ( Fig. 38(b) ), the active metal braze 162 can be applied to the larger diameter end of the opening 158 (i.e., the upper end in Fig. 38(b) ) such that as the active braze 162 flows downwardly, it thins out to ensure even coating on the side walls 160.
  • the pin 22 is then inserted into the opening 158 and the second braze 164 applied ( Fig. 38(e) ). As shown in Fig. 38(e) , if desired the pin 22 may extend completely through the substrate 14 to ensure it is inserted to a sufficient depth.
  • one or the other side 154, 156 of the substrate can be planarized (i.e., by grinding and polishing ( Fig. 38(f) ).
  • the metallization film 88 and bonding materials 90 may then be deposited and the bonding process can be carried out as described above.
  • a solid metal plug formed of the braze materials 162/164 may be formed in the hole 158.
  • the pin 22 may be butt-welded to the plug or attached by various other means.
  • This simple metal filling method may also be utilized where wirebonds or other electrical connections, instead of the pin 22, are desired.
  • the hole 158 may be filled with a conductive cofired metallization in a manner well known in the industry, which results in an appearance similar to Fig. 38(g) .
  • the pin 22 may be attached to the cofired metallization with a braze or other well known methods.
  • the substrate 14 is provided and the openings 158 are formed in the substrate.
  • the premetallization layer 162 (described immediately above and shown in Figs. 37 and 38 ) is then deposited on or adjacent to the openings 158, and the metallization 88 and bonding layers 90 are deposited on circumferential surfaces of the substrate 14 (described in the section entitled "Substrate Attachment” and shown in Fig. 33 ).
  • the substrate 14 is then brazed to the ring 18 (described in the section entitled “Substrate Attachment” and shown in Figs. 34 and 35 ).
  • the pins 22 are brazed to the substrate 14 by braze material 158, as shown in Figs. 37 and 38 either before, after or, at the same time that the substrate 14 is brazed to the ring 18.
  • the sensor die 12 (formed in the section entitled “Sensor Die Manufacturing” and shown in Fig. 17 ) is then attached to the substrate 14, as in the section entitled “Sensor Die Attachment” and shown in Fig. 35 . After the sensor die 12 and substrate 14 are coupled, electrical connections are then completed to the pins 22 and the resultant assembly is then packaged in the base 20 and ring 18 ( Figs. 1 and 6 ).
  • the base 20 includes a backing portion 170 which is located below a substantial portion of the substrate 14 to provide support thereto, and ensures that the substrate 14 can withstand relatively high pressures.
  • the space 171 between the backing portion 170 and the pin 22 may be filled with a high temperature potting compound.
  • the backing portion 170 may be entirely replaced with a high temperature potting compound that substantially fills the space in the metal ring 18 and abuts the lower surface 156 of the substrate 14.
  • the base 20 does not include the backing support portion since the substrate 14 is significantly smaller, and therefore presents less surface area.
  • the metal ring 18 includes a relatively wide foot 172 to allow the ring 18 (and substrate 14) to be securely coupled to the base 20.
  • the portions of the ring 18 (radially) surrounding the substrate 14 may have a relatively small thickness, such that the ring 18 has some compliance and can flex during temperature fluctuations to accommodate any mismatch of the thermal coefficient of expansion between the substrate 14 and ring 18.
  • the flexion of the ring 18 may also provide additional compliance to tolerate thermal expansion and contraction of the base 20.
  • the thickness of the portion of the ring 18 receiving the substrate 14 is determined by the residual stress on the substrate 14 and the amount of stress isolation required between the substrate 14 and the base 20, but in one embodiment is about 0.010 inches thick.
  • the ring 18 should have a relatively low coefficient of thermal expansion to match, as closely as possible, the coefficient of thermal expansion of the substrate 14.
  • the ring 18, and other materials of the packaging having a coefficient of thermal expansion in a given direction that is within about 50%, or about 100%, or about 150% of a coefficient of thermal expansion of the substrate 14 and/or sensor die 12 in the same direction.
  • the materials and shape of the ring 18 are determined based upon the following factors, including but not limited to: relative thermal environment during operation, start-up and cool-down; thermal coefficients of expansion of the base 20 and substrate 14; vibration limits; and the expected maximum and operational pressures and pressure fluctuations.
  • the ring 18 isolates the sensor die 12 and substrate 14 from the base 20 in a cantilever manner such that any stresses applied to or caused by the base 20 are generally not transmitted to the substrate 14.
  • the base 20 and ring 18 may each be made of THERMO-SPAN® metal alloy, sold by CRS Holdings, Inc. of Wilmington, Delaware, which is a controlled expansion alloy which also shows good corrosion resistance.
  • the base 20 and/or ring 18 may be made of stainless steel, INVAR® alloy, a trademark of Imphy S.A. of Paris, France, KOVAR® alloy, NI-SPAN-C® alloy, a trademark of Huntington Alloys Corporation of Huntington, West Virginia, or other material with relatively low coefficients of thermal expansion and corrosion resistance suitable to the environment in which this system will operate.
  • the ring 18 is welded to the base 20 (i.e., at weldments 176 shown in Figs. 1 and 6 ).
  • the components of the base 20 may be coupled by threaded or bolted attachments, and the ring 18 can be coupled to base 20 by a threaded or bolted attachment.
  • a wire 24 (one of which is shown in Figs. 1 and 6 ) is coupled to each of the pins 22 at a coupling location.
  • Each wire 24 can be made of a variety of materials, such as NiCr or platinum with an electrically insulating sheathing.
  • a tip of each wire 24 may be wrapped around the lower end of the associated pin 22, and coupled thereto by a braze attachment.
  • the opposite end of the wire 24 passes through a thermoconductive and electrically insulated material 180, such as a chopped filler material (i.e., NEXTEL® thermal barrier made by 3M of St. Paul, Minnesota or other refractory material) allowing flexibility in the wire assembly 190.
  • the thermoconductive and electrically insulating material 180 is a high temperature ceramic or glass potting compound.
  • a metal (such as nickel or stainless steel) conduit 182 in Fig. 1 is located around the electrically and/or thermally insulating material 180 to provide EMI shielding to the wire(s) 24 located therein.
  • the metal conduit 182 is coupled to a lower port 184 of the base 20 by a braze material 186.
  • Each wire 24 may pass through a single conduit 182, or alternately, each wire 24 may pass through its own dedicated conduit 182.
  • Each wire 24 may be coated with an electrically insulating material and held in place by the insulating material 180.
  • Each conduit 182 may take the form of a rigid conduit, or could take the form of a flexible material such as braided metal wires or the like. When the conduit 182 is a flexible material the braze material 186 may not be utilized, and some other acceptable attachment means would instead be used.
  • the assembly shown in Figs. 39 and 40 illustrates an assembly for electrically connecting the pins 22 to the wires 24.
  • a number of wires 24 i.e., three in the illustrated embodiment
  • Each wire 24 is individually covered in a thermally and electrically insulating sheathing, with the end of each wire 24 being exposed for electrical connection to the associated pin 22.
  • An outer sheath 192 is slidably located on the conduit 190 and flares outwardly from a lower end 194 which is swaged about the conduit 190, to a relative wide mouth 196 which is shaped to mate with the underside of the base 20.
  • each wire 24 is brazed to the associated pin 22 (only one of which is shown in Fig. 39 ).
  • the sheath 192 is then slid upwardly along the conduit 20 until it mates with the base 20, and is then secured to the base, such as by welding 198 ( Fig. 40 ).
  • the sheath 192 is secured, at its opposite end, to the conduit 190 by a braze 200 or the like.
  • the space inside the sheath 192 may be purged with an inert gas, just before sealing, to minimize oxidation.
  • the assembly method of Figs. 39 and 40 provides hermetically sealed electrical connection between the pins 22 and wires 24 with high temperature capability.
  • the assembly also provides a relatively compact packing which allows considerable size reduction in the overall size of the sensor package.
  • the opposite end of the wires 24/conduit 190 may have a second sheath 192 mounted thereon (not shown) to provide protection to the output electrical connections thereof (i.e. connections to a processor or the like).
  • an electronics assembly 202 can be encapsulated in a metal shell 204, with a sheath 196 located at either end thereof. This arrangement permits the electrical connection of two assemblies in a hermetically enclosed metal sheath assembly.
  • the senor 10 and packaging may be used to form a microphone for detecting high frequency pressure fluctuations.
  • the packaging structure disclosed herein can be used with or as part of any high temperature sensor (dynamic or otherwise) including, but not limited to, acceleration, temperature, radiation or chemical sensors.
  • the sensor 10 and packaging may be used to form a chemical detector to detect an analyte present in an environment using either or both electro-chemical sensing or vibration sensing.
  • Such a vibration sensor can, in turn, be used as a component which measures a change in resonance in a variety of manners to detect the presence of ice, contaminants, chemicals, deposition of materials, microorganisms, density of fluids, etc.
  • the transducer and packaging may also be used with or as part of a variety of other types of sensors, such as sensors utilizing piezoresistive or capacitive sensing elements, temperature sensing elements, or the like.
  • the structure shown herein may also be used as a passive structure which can be used, for example, to measure mechanical inputs (i.e., acceleration or vibration) or for use in energy harvesting (i.e., converting vibrations to electrical charge to charge a battery or the like).
  • the thermal protection and isolations features of the actuator packaging described herein lends itself to use in a wide variety of applications and environments, and can be used with a variety of transducers.
  • the piezoresistive transducer of the present invention is in the form of a pressure sensor, generally designated 210.
  • the sensor 210 includes a wafer stack or sensor die 212 (also termed a substrate herein) which includes a base wafer 214, a cap or capping wafer 216 and a device wafer 218 positioned between the base wafer 214 and capping wafer 216.
  • the wafer stack 212 is coupled to a pedestal, header plate, base or header 219, and a frame, cover, package base, pressure case, fitting, or 220 is coupled to the header plate 219 such that the frame 220 and header plate 219 generally encapsulate the wafer stack 212 therein.
  • the lower portion of the frame 220 is often termed a pressure case, and the upper portion of the frame 220 is often termed a vacuum case.
  • the header plate 219 includes a pressure port 222 formed therein with a conduit 224 coupled to the pressure port 222.
  • the pressure port 222 and conduit 224 allows the fluid of interest to exert pressure on a diaphragm 226 (on a first surface of the wafer stack 212) of the device wafer 218.
  • the capping wafer 216 seals the opposite side of the diaphragm 226 (on a second, opposite surface of the wafer stack 212) to provide a reference pressure (or a vacuum) on the opposite surface of the diaphragm 226.
  • a differential pressure across the diaphragm 226 causes the diaphragm 226 to deflect, which deflection is detected by a sensing component 230 located thereon.
  • the output of the sensing component 230 is communicated to an external processor, controller, amplifier or the like via a set of output contacts 232 which are electrically coupled to a set of pins 234.
  • the pins 234 extend through the header plate 219 to thereby communicate the output signals of the sensing component 230 to the processor, controller, amplifier, or the like.
  • the sensing component 230 may include a set of resistors 240 connected together in a Wheatstone bridge configuration.
  • the resistors 240 are coupled to each other, and to the set of output contacts 232, by a set of leads 242.
  • the resistors 240 are positioned on the diaphragm 226 such that two resistors 240 primarily experience mechanical tension when the diaphragm 226 is deflected in a given direction, and the other two resistors 240 primarily experience mechanical compression when the diaphragm 226 is deflected in the given direction.
  • the two pairs of resistors exhibit resistance changes opposite to each other in response to a deflection of the diaphragm 226.
  • the resistance change is then amplified in the well-known manner of a Wheatstone bridge.
  • the two pairs of resistors may exhibit opposite resistance changes due to their positioning on the diaphragm 226, or due to their orientation of directional dependent resistance characteristics thereof.
  • the resistors 240 may be made of doped silicon, such as p-doped or n-doped single crystal silicon.
  • the configuration shown in Figs. 43 and 44 may be utilized.
  • the resistors 240 are formed of n-doped silicon, the configuration shown in Fig. 45 may be utilized, wherein the resistors 240 are rotated about 45 degrees from their positions in Fig. 44 due to differing directional sensitivity of n-doped silicon as compared to p-doped silicon. Because the resistors 240 of Fig. 45 are rotated 45 degrees, the resistors 240 of Fig. 45 may be more difficult to form when using photolithography.
  • p-type resistors are typically less temperature dependent than n-type resistors and therefore p-type resistors may be desired to be utilized.
  • the output contacts 232 and leads 242, or parts thereof, may be formed of the same material as the resistors 240 (i.e., doped silicon).
  • a temperature sensor 231, such as a temperature-sensitive resistor, may be located on the device wafer 218, with a pair of output contacts 232 coupled via leads to opposite sides of the temperature sensor 231.
  • the temperature sensor 231 allows the controller, processor amplifier to use temperature-compensating techniques when analyzing the output of the sensing component 230.
  • Figs. 46-56 One process for forming the wafer stack 212 of Fig. 42 is shown in Figs. 46-56 and described below, although it should be understood that different steps may be used in the process, or an entirely different process may be used without departing from the scope of the invention. Thus, the manufacturing steps illustrated here are only one manner in which the wafer stack 212 may be manufactured, and the order and details of each step described herein may vary, or other steps may be used or substituted with other steps that are well known in the art. A batch manufacturing process may be utilized, but for clarity of illustration, Figs. 46-56 illustrate only a single wafer stack 212 being formed.
  • Figs. 46-56 represent a schematic cross-section of a wafer during manufacturing, and the location of certain components may not necessarily correspond to a true cross section.
  • the process begins with a semiconductor-on-insulator wafer 244 such as a double sided polished three inch or four inch diameter (or larger) semiconductor-on-insulator or silicon-on-insulator wafer.
  • the SOI wafer 244 includes a base or bulk layer 246 and a device layer 248, with an electrically insulating layer 250 positioned therebetween.
  • the device layer 248 is single crystal silicon having a thickness of about 0.34 microns, although the device layer 248 may have a variety of thicknesses, such as between about 0.05 microns and about 1 microns, or less than about 1 micron, or less than about 1.5 microns, or, or less than about 0.5 microns, or greater than about 0.05 microns. Because the thickness of the device layer 248 will ultimately determine the thickness of the resistors 240, the thickness of the device layer 248 should be carefully selected (although the thickness of the device layer 248 could be reduced during later processing steps, if desired).
  • the device layer 248 may have a (100) crystal orientation. If desired, the device layer 248 can be made of other materials that are piezoresistive or can be made piezoresistive, such as polysilicon or silicon carbide. When the device layer 248 is made of single crystal semiconductor materials (i.e., silicon), as opposed to polysilicon, defects in the device layer 248 caused by grain growth and doping segregation in the grain boundaries are avoided.
  • single crystal semiconductor materials i.e., silicon
  • the thin device layer may be formed from a thicker, starting wafer (not shown) by bombarding the face of the thicker wafer with ions to define a sub-layer of gaseous microbubbles. The thicker wafer is then separated along the line of microbubbles to provide the thin device layer 248, which is then deposited on the insulating layer 250 to form the SOI wafer 244.
  • a thicker, starting wafer not shown
  • the thicker wafer is then separated along the line of microbubbles to provide the thin device layer 248, which is then deposited on the insulating layer 250 to form the SOI wafer 244.
  • the device layer 248 may be formed or provided by hydrogen ion delamination of the thicker wafer.
  • This method of forming the wafer 244 provides a device layer 248 having a uniform thickness, which increases product yield.
  • This method of forming the wafer also provides excellent doping uniformity and allows the use of silicon which has improved high temperature thermal stability as compared to, for example, polysilicon.
  • the base layer 246 can be made of a variety of materials, such as silicon or the other materials listed above for the device layer 248.
  • the base layer 246 can have a variety of thicknesses such as between about 100 microns and about 1,000 microns, and more particularly, about 500 microns.
  • the base layer 246 should be of sufficient thickness to provide structural support to the wafer 244.
  • the base layer 246 is single crystal silicon having a (100) crystal orientation to allow easy etching thereof.
  • the insulating layer 250 can be of any variety of materials, and is typically silicon dioxide.
  • the insulating layer 250 primarily acts as an etch stop and also provides electrical isolation to the wafer 244.
  • the insulating layer 250 also enables the sensor 210 to function at very high temperatures without leakage effects associated with the p-n junction type devices (i.e. due to current passing through the base layer 246).
  • the insulating layer 250 may have a variety of thicknesses, such as between about 0.5 microns and about 1.5 microns, and is typically about 1 micron thick.
  • a thermal oxide 252 such as a 200 Angstroms thick thermal oxide layer, is deposited or grown on top of the device layer 248 and on the bottom of the wafer 244 ( Fig. 47 ) to aid in subsequent doping.
  • the device layer 248 is then doped (schematically shown by arrows in Fig. 47 ) by either p-doping or n-doping, although p-doping may provide certain benefits as outlined above.
  • the device layer 248 may be doped to its highest level of solubility, and the doping may be carried out by a variety of methods, such as by high-dose ion implantation or boron diffusion. In one example the device layer 248 may have a post-doping resistance of between about 14 and about 30 ohm-cm.
  • the wafer 244 is then annealed to complete the doping process.
  • the wafer 244 is annealed at a temperature of about 1050°C in an atmosphere of N 2 for about 15 minutes.
  • a mask material 254 such as silicon nitride, is deposited on both sides of the wafer 244 by low pressure chemical vapor deposition ("LPCVD") or other suitable deposition process.
  • the silicon nitride 254 can have a variety of thicknesses, and in one example is about 1500 Angstroms thick.
  • the upper layer of silicon nitride 254 is then patterned (or deposited in a patterned shape) in the desired shape of the resistors 240, output contacts 232, and leads 242 as schematically shown in Fig. 49 .
  • the exposed portions of the device layer 248 are then removed.
  • the upper layer of silicon nitride 254 is then removed to expose the remaining portions of the device layer 248 as shown in Fig. 50 .
  • a silicon dioxide 258 is then coated on top of the wafer 244, such as by PECVD. Portions of the silicon dioxide 258 are then removed ( Fig. 52 ) to expose part of the output contacts 232 lying below such that output contacts 232 can be completed. Portions of the silicon dioxide 258 and the insulating layer 250 are also removed at the area indicated 231 to expose the base layer 246 to provide a location for a substrate contact 260 (see Figs. 42 and 53 ). The substrate contact 260 provides an electrical contact to the base layer 246 to avoid voltage build-ups on the wafer 244/sensor die 212, thereby reducing noise.
  • a metallization layer is then deposited in the openings of the silicon dioxide 258 to form/complete the substrate contact 260 and output contacts 232.
  • the metallization layer may be the same metallization layer 88 described above in the section entitled "Metallization Layer.”
  • the metallization layer 88 as deposited, includes a lower layer of tantalum, with a layer of tantalum nitride located on the tantalum layer, and a top layer of platinum located on the tantalum nitride layer.
  • the metallization layer 88 may be patterned by a lift-off resist ("LOR") or by a shadow masking sputter technique.
  • the metallization layer 88 provides a surface which can withstand elevated temperatures and can still be welded to after such exposure to elevated temperatures.
  • the metallization layer 88 may be exposed to elevated temperatures when the base wafer 214, device wafer 218 and capping wafer 216 are coupled together, and when the wafer stack 212 is coupled to the header plate 219.
  • the make-up of the metallization layer 88 allows it to remain sufficiently conductive, retain its adhesive strength, and remain metallugically stable after exposure to such temperatures, and when exposed to elevated temperatures during operation of the sensor 210.
  • the thermal oxide 252 on the bottom of the wafer 244 is patterned to expose a portion of the base layer 246 located below the resistors 240.
  • the exposed portion of the base layer 246 is then etched to define the diaphragm 226 and a cavity 262 located below the diaphragm ( Fig. 55 ).
  • This etching step can be carried out by DRIE, a KOH etch, or any of a variety of other etching methods.
  • the bottom layer thermal oxide 252 is then removed.
  • the diaphragm 226 can have a variety of shapes, such as circular or square in top view, and in one example has a surface area of between about 0.25 mm 2 and about 9 mm 2 .
  • the diaphragm 226 may be etched to a thickness of between about 1 micron and about 200 microns, or less than about 200 microns, or greater than about 1 micron, or greater than about 8 microns, or greater than about 30 microns, or less than about 150 microns.
  • the wafer 244 includes an additional buried oxide layer 264.
  • the buried oxide layer 264 may be utilized as an etch stop during the etching of the base layer 246 to form the diaphragm 226. In this manner, the buried oxide layer 264 helps to ensure a consistent diaphragm 226 thickness.
  • the exposed portions of the oxide layer 264 may be removed to reduce thermal stresses imposed on the diaphragm 226 by the oxide layer 264.
  • the base wafer 214 is then provided ( Fig. 56 ).
  • the base wafer 214 may be a 800 micron-thick silicon wafer that is KOH etched to form a through-hole 265.
  • the capping wafer 216 is also provided, and may be a silicon wafer that is KOH or DRIE etched to form a cavity 266.
  • the wafer stack 212 is then formed by coupling the base wafer 214, device wafer 218 and capping wafer 216 together.
  • the wafers 214, 216, 218 are aligned and are coupled together using a glass frit attachment layer 221 ( Fig. 56 ) or other acceptable joining methods. Glass frit attachment provides a well tested and predictable attachment method.
  • Plasma enhanced fusion bonding may also be utilized to bond the wafer stack 212. Plasma enhanced fusion bonding allows the wafer stack 212 to be formed at a temperature as low as 300°C, which can reduces damage to the electronics/piezoresistive materials.
  • the stack 212 is coupled to the header plate 219, such as by an InCuAg brazing material 270 (see Fig. 42 ) formed at a bonding temperature of about 750°C.
  • an InCuAg brazing material 270 (see Fig. 42 ) formed at a bonding temperature of about 750°C.
  • other high temperature braze materials may be utilized, such as other eutectic bonding materials (i.e. a gold/germanium eutectic), or a conductive glass transfer tape having a firing temperature of 440°C or higher, nonconductive glass frit with a firing temperature of 600°C or higher, or an InCuAg alloy based brazing preform with a eutectic liquid temperature of 705°C or higher.
  • a L10102 glass frit with a curing temperature of between 600°C and 650°C may also be used.
  • the material attaching the stack 212 to the pedestal may be able to withstand more than 800 psig at 500°C
  • the glass transfer tape used as attachment material 270 may be of a standard sandwich-type construction including a bottom polyethylene carrier strip, a glass layer located on tope of the carrier, an organic adhesive layer on top of the glass layer, and a top layer of release paper.
  • the bond 270 may be formed at a curing temperature between about 600°C and about 650°C, and has stable mechanical properties at about 400°C, or about 500 °C or at about 550°C.
  • the metallization layer 88 has good adhesion to silicon and stable electrical properties at temperatures up to 600°C and is able to withstand temperatures at least up to 725° or 750°C. Thus the metallization layer 88 should be able to survive the attachment of the wafers 214, 216, 218 together, as well as the attachment of the wafer stack 212 to the header plate 219.
  • the wafer stack 212 may be formed by joining the base wafer 214 and device wafer 218 and/or device wafer 218 and capping wafer 216, by relatively high temperature bonding processes.
  • the bonding temperatures may be sufficiently high that the metallization layer 88 or other sensitive components on the wafer stack 212 cannot withstand the high temperature.
  • the metallization layer 88 may be deposited after the wafer stack 212 is partially or completely formed (i.e., after the base wafer 214 and device wafer 218, and/or device wafer 218 and capping wafers 216 have been joined).
  • the sensor 210 includes a plurality of pins 234, with each pin 234 being coupled to an output contact 232 by a wire 272 to communicate the output of the sensor 210.
  • the wires 272 may be made of platinum and have a diameter of between about 25 and about 75 microns.
  • Each wire 272 may be spot welded or wedge bonded (i.e. both considered "wire bonding" for the purposes of this application) to the platinum pins 234 at one end, or to an associated output contact 232 at the other end thereof.
  • Wedge bonding is a well known process and comprises pressing the wire 272 onto the surface to be welded and applying ultrasonic energy to complete the bond.
  • the pins 234 can be made of a variety of materials, such as platinum coated KOVAR® alloy or solid platinum. When the pins 234 are solid platinum, instead of platinum plated, any diffusion of nickel, which can compromise the joint between the wire 272 and pin 234, is eliminated. In addition, when the wires 272 are platinum, instead of the traditional gold material, platinum-to-platinum wire bonds can be utilized (since the top surface of the metallization 88 may be primarily platinum due to a gradient of platinum silicide in the top layer 110). If the wires 272 were to be made of gold, the gold may migrate and form a gold-silicon eutectic which causes the wires 272/output contacts 232 to become brittle and fail at high temperatures. Thus the platinum-to-platinum wire bonds allows the connections to take advantage of the natural ability of platinum to withstand high temperatures and corrosive environments.
  • a plurality of pins 234 are mounted in the header plate 219 and extend therethrough, and are held in place by ceramic, ceramic glass or glass frit material 276 or other acceptable material.
  • ceramic or glass frit feed through 276 provides materials which can withstand higher temperatures as contrasted with glass feed through material.
  • glass frit or ceramic feed throughs 276 are more compatible with platinum than glass pin seals.
  • the header plate 219 and/or frame 220 can be made of a variety of materials, such as stainless steel, INVAR® alloy, KOVAR® alloy, NI-SPAN-C® alloy, aluminum nitride, or other corrosion resistant materials with relatively low coefficients of thermal expansion.
  • the header plate 219 and frame 220 can be welded or threaded together.
  • the header plate 219 shown in Fig. 42 can be replaced with the pedestal assembly 280 of Fig. 57 .
  • the pedestal assembly 280 may include a ceramic substrate 282, which can be made of the materials described above for the substrate 14.
  • the substrate 282 may be compression mounted inside a ring 284, in the same manner described above in the section entitled "Substrate Attachment.”
  • a set of pins 234 may be mounted in and through the substrate 282. A variety of methods for mounting the pins 234 may be utilized, but in one example the mounting process described above in the section entitled "Pin Mounting" may be utilized.
  • a conduit 286 may be mounted in and through the substrate 282 to communicate the pressure-conveying fluid to the underside of the diaphragm 226.
  • the conduit 282 can be mounted in and to the substrate 282 in the same manner as the pins 234, and its upper end is planarized and polished flat to allow the sensor die 212 to be attached thereto.
  • the sensor die 212 can be attached to the pedestal assembly 280 by, for example, glass frit or a gold-germanium (or other material) transient liquid phase bond.
  • the wires 272 of Fig. 42 can be attached to the pins 234, and the pedestal assembly 280 can be coupled to the frame 220 in the same or similar manners as the pedestal/header plate 219 of Fig. 42 .
  • the pedestal assembly 280 may be able to accommodate higher temperatures due to the use of a ceramic substrate 282, and may be easier to manufacture.
  • the sensing component 230 is made of or includes piezoresistive material.
  • the sensing component 230 may be made of or include piezoelectric material, in the same or similar manner to the sensors 10 described in detail above (i.e. in Figs. 8-17 and the accompanying description) which results in a dynamic pressure sensor.
  • the piezoresistive material in the example and embodiment described below (“Piezoresistive Transducer - Second example” and “Piezoresistive Transducer - Embodiment”) may also be replaced with piezoelectric material to result in piezoelectric transducers.
  • sensors/transducers described in these sections may have increased utility as piezoresistive sensors/transducers, rather than piezoelectric sensors/transducers, and thus the headings refer to those transducers as “piezoresistive” rather than “piezoelectric.”
  • a second example of the piezoresistive transducer is 292 is shown in Figs. 58-60 .
  • the sensor die 290 is mounted on an opposite side of the header plate 219 relative to the pins 234 and compared to the example of Fig. 42 .
  • the pressure exerted on the diaphragm 226 tends to pull the sensor die 212 away from the header plate 219.
  • pressure applied to the sensor die 290 pushes the attachment joint 270 in compression and thereby greatly increases the burst pressure of the pressure sensor 292.
  • the sensor die 290 of the example of Figs. 58-60 may have generally the same structure as, and be formed in the same manner as, the sensor die 212 of the example of Figs. 42-56 . However, the sensor die 290 of Figs. 58-60 may not include the base wafer 214. In addition, as can be seen in Figs. 58 and 59 , the capping wafer 216 may generally cover the device wafer 218 and have a pair of slots 294 formed therethrough to provide access to the output contacts 232. Each wire 272 also passes through an opening 309 formed in the header plate 219 to access an output contact 232.
  • a vacuum/inert gas or reference pressure may be sealed in the cavity 266 between the capping wafer 216 and die wafer 218.
  • a vacuum, inert gas or reference pressure may be sealed in the cavity 300 located between the capping wafer 216 and the header plate 219.
  • the capping wafer 216 may include an opening formed therein (not shown) such that the two cavities 266, 300 communicate.
  • a vacuum, inert gas or reference pressure may be present in the cavity 302 located between the frame 220 and the header plate 219, and this cavity 302 could communicate with the other two cavities 300, 266.
  • the pins 234 are mounted in holes in the header plate 219 that only extend partially therethrough. The blind mounting of the pins 234 ensures that the cavity 302 defined by the header plate 219 and frame 220 is not compromised.
  • the pins 234 may be attached by a glass frit or ceramic feed through material 276 as in the example of Fig. 42 .
  • the pressure port 224 is on the bottom side of the sensor die 290 and all electrical connections can be protected in the vacuum or nitrogen environment in the cavities 206, 300, 302 to prevent contamination and/or oxidation of the sensor elements and electrical connections.
  • Each pin 234 is electrically coupled to an associated tubular feedthrough 306 by a platinum wire 308 to communicate the output of the sensor 292.
  • Each tubular feedthrough 306 is coupled to the upper end of the cover 220 and may be made of platinum.
  • the tubes 306 may be positioned inside a larger tube or shell 309 that is coupled to an upper end of the frame 220 by brazing or the like.
  • the shell 309 is filled with a ceramic material, or glass frit, or a potting compound 310, and each tube 306 is coupled to the material 310 by brazing or the like.
  • Each wire 308 may be brazed to an associated tube 306 at an upper end of that wire 308 and to an associated pin 234 at the other end.
  • a plug material 312, such as ceramic, may be inserted into each tube 306 to seal off the tubes 306.
  • a vacuum seal tube 315 may be positioned adjacent to the tubes 306 to allow the cavities 302 and/or 300 and/or 266 to be evacuated to provide absolute pressure measurements. The vacuum seal tube is sealed to seal out the ambient environment.
  • tube arrangement 306 shown in Fig. 60 may be used with a variety of other sensors and packaging for providing an exit path of the wires 308, for example, the tube arrangement can be used with piezoelectric sensors and associated packaging shown in Figs. 1 and 6 .
  • the header plate 219 can be made of a variety of materials, such as KOVAR®, AlN or other high temperature resistant, corrosion resistant materials as described above, and the material may be selected such that its thermal expansion coefficient ("TEC") is relatively close to that of silicon.
  • TEC thermal expansion coefficient
  • a pair of stress isolator rings 314 are located on either side of the header plate 219.
  • the stress isolator rings 314 can be made of a variety of materials, such as KOVAR®, stainless steel or other materials similar to the header plate 219. Each of the stress isolator rings 314 may be received in a groove on the top or bottom surface of the header plate 219 and welded to the pressure case 220.
  • Each stress isolator ring 314 may have a relatively thin wall thickness (i.e., about 10 mils) to allow each stress insulator ring 314 to expand or flex to accommodate thermal mismatches in the sensor package/assembly.
  • the KOVAR® materials of the header plate 219 and/or rings 314 could be replaced with THERMO-SPAN® or other controlled expansion, high temperature resistant material.
  • FIG. 61-65 An embodiment of the sensor of the present invention is shown in Figs. 61-65 .
  • the device wafer 320 that is the same as or similar to the device wafer 218 described above, may be utilized.
  • the device wafer 320 may also be formed by the process shown in Figs. 46-55 and the accompanying description.
  • the device wafer 320 is mechanically and electrically coupled to an adjacent substrate 322.
  • the device wafer 320 is attached in an inverted configuration, as in the second example described above, to improve the ability of the sensor 324 to accommodate high pressures.
  • a reference pressure or vacuum or inert gas may be located in the cavity 325 positioned between the substrate 322 and the frame 220, and/or the cavity 326 between the substrate 322 and the device wafer 320. Furthermore, if desired, an opening 319 may be formed in the substrate 322 to allow the cavities 325, 326 to communicate.
  • the device wafer 320 includes a frame 340 that extends around the perimeter thereof, as well as a pair of bulkheads 342 extending laterally across the device wafer 320.
  • the frame 340 and bulkheads 342 may be made of the metallization material 88 and the bonding layer 90 described above. In this sense the frame 340 and bulkheads 342 may be made of the same material as the frame 70 and bulkhead 72 of the device wafer shown in Fig. 3 .
  • the substrate 322 includes a frame 344 and bulkhead 346 that generally match (in size and shape) the frame 340 and bulkheads 342 of the device wafer 320 of Fig. 62 .
  • the frame 344 and bulkheads 346 can also be made of the metallization layer 88 with the bonding layer 90 on top thereof.
  • the substrate 322 also includes a set of contacts 348 that are configured to align with the output contacts 232 of the device wafer 320. In this sense the substrate 322 is analogous to the substrate 14 described and shown above.
  • the device wafer 320 and substrate 322 In order to join the device wafer 320 and substrate 322, they are aligned as shown in Fig. 64 such that their frames 340, 344, bulkheads 342, 346, and contacts 232, 348 are aligned. The device wafer 320 and substrate 322 are then pressed into contact such that the frames 340, 344, bulkheads 342, 346 and contacts 332, 348 contact each other. The device wafer 320 and substrate 322 are next joined or bonded in a transient liquid phase bonding process which is described above in the section entitled "Sensor Die Attachment.” The resultant structure is shown in Fig. 65
  • the frame 310, 344 and bulkheads 342, 346 provide sealed cavities around the contacts 232, 378.
  • the sealed cavities isolate the electrical portion of the device (i.e., the contacts 232) from the pressure portion (i.e., the diaphragm 226) to ensure that the pressure medium does not invade and contaminate/corrode the electrical elements or components, and also protects the electrical elements and components from high pressures.
  • the substrate 322 may be a generally disk-shaped ceramic material that is made of the same materials as the substrate 14 described above.
  • the substrate 322 may be compression mounted inside a thin walled metal ring 18 (i.e., in the same manner as described above in the section entitled "Substrate Attachment").
  • the ring 18 is, in turn, mounted to the frame 220 which provides support to the ring 18 and structure and protection to the sensor 324 as a whole.
  • a set of pins 234 are electrically coupled to the device wafer 320 at one end, and to an associated wire 308 at the other end thereof.
  • Each pin 234 may be coupled to the substrate 322 as described above in the section entitled "Pin Mounting" above.
  • Each wire 308 is coupled to, or extends through, a tube 306 at the other end similar to the example shown in Fig. 60 .
  • wire bonding to the contact pads 232 is eliminated.
  • a flip-chip process which is more automated, controlled and predictable, is used to complete electrical connections to the contact pads 232 and pins 234.
  • Fig. 66 illustrates another example that is somewhat of a "hybrid" between the sensor of Figs. 58-60 and the sensor of Figs. 61-65 .
  • the sensor die 290 may be similar to the sensor die 290 of the example of Figs. 58-60 .
  • the header plate 219 can be made of a variety of materials, such as AlN, KOVAR®, or other high temperature resistant, corrosion resistant materials as described above.
  • the output contacts 232 are coupled to the pins 234 by (platinum) wires 272.
  • the header plate 219 is compression mounted inside the ring 18, and the pins 234 are planarized and brazed in place similar to the pins 234 shown in Fig. 61 .
  • This example combines the predictable technology of wire bonding with the advantages of a compression mounted, isolated header plate 219.
  • each example or embodiment may be designed to withstand a pressure up to 600 psig, or 800 psig.
  • the first example may be able to withstand a pressure of up to 600 psig and a temperature up to 5000C.
  • the second and hybrid examples and the embodiment may be able to withstand a pressure of up to 4000 psig and a temperature up to 4500C or up to 5000C.
  • the sensor of the various examples and the embodiment may also be able to withstand corrosive environments - for example, direct exposure to combustion byproducts, for an extended period of time (i.e. up to 40 hours, or up to 400 hours, or up to 4,000 hours) and continue functioning such that the sensor can be used in or adjacent to a combustion zone.
  • the various piezoresistive and piezoelectric pressure sensors disclosed herein may also, if desired, take the form of various other pressure sensors that are not limited to piezoresistive and/or piezoelectric sensing elements.
  • the packaging, metallization, joining, pin mounting and other features disclosed herein may be utilized with such pressure sensors.
  • the various features disclosed herein are not necessarily restricted to use with pressure sensors, and can be used with any of a wide variety of sensors and transducers as disclosed in, for example, the section entitled "Field of Use" described above.

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Claims (15)

  1. Capteur de pression destiné à être utilisé dans un environnement hostile comprenant :
    un substrat (14) ;
    une puce de capteur (12) couplée directement audit substrat (14) par un cadre de liaison (70) positionné entre ledit substrat (14) et ladite puce de capteur (12), ladite puce de capteur (12) incluant une membrane généralement flexible (16) configurée pour se fléchir lorsqu'une pression différentielle suffisante est appliquée sur toute la membrane ;
    un élément de détection piézoélectrique ou piézorésistif (40) au moins situé en partie sur ladite membrane (16) de sorte que ledit élément de détection (40) délivre un signal électrique lors de la flexion de ladite membrane (16) ;
    un contact de sortie (50, 52, 60) situé sur ladite puce de capteur (12) et électriquement couplé audit élément de détection, dans lequel ledit cadre de liaison s'étend autour du périmètre de ladite puce de capteur (12) et dudit contact de sortie (50, 52, 60), et inclut également une cloison (72) s'étendant latéralement à travers ladite puce de capteur (12), ledit cadre de liaison (70) et ladite cloison (72) formant une cavité scellée (76) autour dudit contact de sortie (50, 52, 60), dans lequel ladite cavité scellée (76) est isolée de manière fluidique de ladite membrane (16) ; et
    un composant de connexion (22) électriquement couplé audit contact de sortie (50, 52, 60) à un emplacement de connexion (57) qui est isolé de manière fluidique de ladite membrane (16) par ledit cadre de liaison (70) et par ladite cloison (72), dans lequel ledit cadre de liaison (70) est fait de matériaux et ledit composant de connexion (22) est électriquement couplé audit élément de détection (40) par les mêmes matériaux dudit cadre de liaison (70).
  2. Capteur selon la revendication 1 dans lequel ledit cadre de liaison (70) est situé autour dudit emplacement de connexion (57) de sorte que ledit cadre de liaison, ladite cloison (72), ledit substrat (14) et ladite puce de capteur (12) forment une cavité généralement scellée autour dudit emplacement de connexion.
  3. Capteur selon la revendication 1 dans lequel lesdits matériaux dudit cadre de liaison (70) sont fabriqués selon un processus de liaison à une température de liaison, et lesdits matériaux dudit cadre de liaison (70), après ledit processus de liaison, ne fondent pas lorsqu'ils sont soumis à ladite température de liaison.
  4. Capteur selon la revendication 1 dans lequel lesdits matériaux dudit cadre de liaison (70) sont fabriqués selon un processus de liaison eutectique en phase liquide transitoire à une température de liaison de moins de 500 degrés Celsius, et lesdits matériaux dudit cadre de liaison (70), après ledit processus de liaison, ne fondent pas lorsqu'ils sont soumis à des températures dépassant 600 degrés Celsius.
  5. Capteur selon la revendication 1 dans lequel ledit substrat (14) inclut une ouverture et ledit composant de connexion (22) s'étend à travers l'ouverture et est directement couplé audit substrat au niveau de ladite ouverture.
  6. Capteur selon la revendication 1 dans lequel ledit élément de détection (40) inclut un film piézoélectrique (42) situé sur ladite membrane (16), une électrode (44, 46) située sur ledit film piézoélectrique (42) et sur ladite membrane (16), et un fil (56, 58) électriquement couplé à ladite électrode (44, 46) à une extrémité et électriquement couplé audit composant de connexion (22) audit emplacement de connexion (57) à une autre extrémité.
  7. Capteur selon la revendication 6 dans lequel au moins une partie dudit fil (56, 58) est positionnée directement entre ledit cadre de liaison (70) et ladite puce de capteur (12).
  8. Capteur selon la revendication 1 dans lequel ledit composant de connexion (22) est électriquement couplé audit élément de détection (40) par un moyen de connexion, dans lequel ledit moyen de connexion est fabriqué selon un processus de liaison eutectique en phase liquide transitoire exécuté à une première température, et dans lequel ledit moyen de connexion, après ledit processus de liaison, ne fond plus lorsqu'il est soumis à une seconde température qui est supérieure à ladite première température.
  9. Capteur selon la revendication 1 dans lequel ledit contact de sortie (50, 52, 60) et ledit cadre de liaison (70) comprennent tous deux un alliage eutectique de solution solide.
  10. Capteur selon la revendication 9 dans lequel une couche de métallisation (88) est positionnée sur chaque côté dudit alliage eutectique de solution solide et située immédiatement adjacente audit alliage eutectique de solution solide, et dans lequel au moins une couche de métallisation (88) inclut une couche d'adhésion (102) sélectionnée dans le groupe constitué de composés qui sont le produit de réaction de la puce de capteur ou du substrat et d'un métal sélectionné dans le groupe constitué de tantale, de chrome, de zirconium et de hafnium, une première couche de blocage de diffusion (104) d'un composé sélectionné dans le groupe constitué de siliciure de tantale, de carbure de tantale, de nitrure de tantale et de nitrure de tungstène, et une seconde couche de blocage de diffusion (106) de siliciure de platine.
  11. Capteur selon la revendication 1 dans lequel ledit substrat (14) est fait d'un matériau céramique et est positionné à l'intérieur d'un anneau en métal (18), et dans lequel ledit substrat (14) est brasé audit anneau par un cordon de brasure, et dans lequel le cordon de brasure inclut une couche de métallisation (88), ladite couche de métallisation incluant une couche d'adhésion sélectionnée dans le groupe constitué de composés qui sont le produit de réaction du substrat et d'un métal sélectionné dans le groupe constitué de tantale, de chrome, de zirconium et de hafnium, une première couche de blocage de diffusion d'un composé sélectionné dans le groupe constitué de siliciure de tantale, de carbure de tantale, de nitrure de tantale et de nitrure de tungstène, et une seconde couche de blocage de diffusion de siliciure de platine.
  12. Capteur selon la revendication 1 dans lequel ledit substrat (14) est fait d'un matériau céramique et est positionné dans un anneau (18), et dans lequel ledit substrat est maintenu dans un état de compression à l'intérieur dudit anneau.
  13. Capteur selon la revendication 1 dans lequel ladite puce de capteur (12) est un matériau isolant sur silicium ayant une couche de dispositif de silicium située sur une couche d'isolant, et dans lequel ladite couche de dispositif est (111) du silicium, et dans lequel ledit élément de détection (40) inclut un film piézoélectrique (42) obtenu par croissance épitaxiale sur ladite couche de dispositif.
  14. Capteur selon la revendication 13 dans lequel ledit film piézoélectrique (42) est du nitrure d'aluminium et ladite membrane (16) est du silicium et a une épaisseur entre environ 3 et environ 300 microns.
  15. Capteur selon la revendication 1 dans lequel ladite membrane (16) est généralement exposée à la même pression statique sur chacune de ses faces de sorte que ladite membrane est généralement équilibrée de manière hydrostatique.
EP07814915.0A 2006-09-19 2007-09-19 Transducteur destiné à être utilisé dans des environnements hostiles Active EP2082205B1 (fr)

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Application Number Priority Date Filing Date Title
US11/523,214 US7538401B2 (en) 2005-05-03 2006-09-19 Transducer for use in harsh environments
PCT/US2007/078837 WO2008036705A2 (fr) 2006-09-19 2007-09-19 Transducteur destiné à être utilisé dans des environnements hostiles

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EP2082205A2 EP2082205A2 (fr) 2009-07-29
EP2082205B1 true EP2082205B1 (fr) 2016-06-29

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US20110256652A1 (en) 2011-10-20
US7538401B2 (en) 2009-05-26
US7642115B2 (en) 2010-01-05
EP2082205A2 (fr) 2009-07-29
US7952154B2 (en) 2011-05-31
US20090203163A1 (en) 2009-08-13
US20100155866A1 (en) 2010-06-24
US20100065934A1 (en) 2010-03-18
US8013405B2 (en) 2011-09-06
WO2008036705A3 (fr) 2009-04-09
WO2008036705A2 (fr) 2008-03-27
US20090108382A1 (en) 2009-04-30
US8460961B2 (en) 2013-06-11
JP2010504529A (ja) 2010-02-12

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